Lanthanum carbonate chewable tablets are phosphate binder indicated to reduce serum phosphate in patients with end- stage renal disease (ESRD). Management of elevated serum phosphorus levels in patients with ESRD usually includes all of the following: reduction in dietary intake of phosphate, removal of phosphate by dialysis, and reduction of intestinal phosphate absorption with phosphate binders.
Divide the total daily dose of lanthanum carbonate chewable tablets and take with or immediately after meals. The recommended initial total daily dose of lanthanum carbonate chewable tablets is 1,500 mg. Titrate the dose every 2 to 3 weeks until an acceptable serum phosphate level is reached. Monitor serum phosphate levels as needed during dose titration and on a regular basis thereafter. Lanthanum Carbonate chewa...
Lanthanum carbonate is supplied as chewable tablets in three dosage strengths for oral administration: 500-mg tablets, 750-mg tablets, and 1000-mg tablets. Each 500-mg chewable tablet is off-white to yellowish white, round flat faced bevel edge debossed “IG” on one side with “476” on the other. 500- mg Patient Pack (2 bottles of 45 tablets, NDC 69097-934-57, per each patient pack) NDC 69097-934-98 Each 750-mg chew...
www.fda.gov/medwatchLanthanum carbonate chewable tablets are phosphate binder indicated to reduce serum phosphate in patients with end- stage renal disease (ESRD).
Management of elevated serum phosphorus levels in patients with ESRD usually includes all of the following: reduction in dietary intake of phosphate, removal of phosphate by dialysis, and reduction of intestinal phosphate absorption with phosphate binders.
Divide the total daily dose of lanthanum carbonate chewable tablets and take with or immediately after meals. The recommended initial total daily dose of lanthanum carbonate chewable tablets is 1,500 mg. Titrate the dose every 2 to 3 weeks until an acceptable serum phosphate level is reached. Monitor serum phosphate levels as needed during dose titration and on a regular basis thereafter.
Lanthanum Carbonate chewable Tablets has the potential to bind other orally administered drugs; consider separating the administration of other oral medications [see Drug Interactions (7)].
In clinical studies of patients with ESRD, lanthanum carbonate chewable tablets doses up to 4,500 mg were evaluated. Most patients required a total daily dose between 1,500 mg and 3,000 mg to reduce plasma phosphate levels to less than 6.0 mg/dL. Doses were generally titrated in increments of 750 mg/day.
Information for lanthanum carbonate chewable tablets
Chew or crush lanthanum carbonate chewable tablets completely before swallowing. Do not swallow intact lanthanum carbonate chewable tablets.
Consider using the oral powder formulation in patients with poor dentition or who have difficulty chewing tablets.
Lanthanum carbonate chewable tablets: 500 mg, 750 mg, and 1,000 mg.
Contraindicated in patients with:
• hypersensitivity to Lanthanum carbonate or to any ingredient in the formulation. (4)
• bowel obstruction, including ileus and fecal impaction.
Serious cases of gastrointestinal obstruction, ileus, subileus, gastrointestinal perforation, and fecal impaction have been reported in patients taking lanthanum, some requiring surgery or hospitalization.
Consider discontinuing lanthanum carbonate in patients without another explanation for severe gastro intestinal symptoms.
Risk factors for gastrointestinal obstruction and gastrointestinal perforation identified from post-marketing reports in patients taking lanthanum carbonate chewable tablets include abnormal gastrointestinal anatomy (e.g., diverticular disease, peritonitis, history of gastrointestinal surgery, gastrointestinal cancer, gastrointestinal ulceration), hypomotility disorders (e.g., constipation, ileus, subileus, diabetic gastroparesis) and the use of medications known to potentiate these effects. Some cases were reported in patients with no history of gastrointestinal disease.
Patients with acute peptic ulcer, ulcerative colitis, Crohn’s disease, or bowel obstruction were not included in lanthanum carbonate clinical studies [see Contraindications (4).]
Advise patients who are prescribed lanthanum carbonate chewable tablets to chew the tablet completely and not to swallow them whole. Serious gastrointestinal complications have been reported in association with unchewed or incompletely chewed tablets.[see Adverse Reactions (6.2)]
Lanthanum carbonate chewable tablet has radio-opaque properties and therefore may give the appearance typical of an imaging agent during abdominal X-ray procedures. Postmarketing reports of product residue have been reported during endoscopic imaging.
The following adverse reactions are discussed in greater detail in other sections of the labeling:
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
Overall, the safety profile of Lanthanum carbonate chewable tablets has been studied in over 5,200 subjects in completed clinical trials. The most common adverse reactions for lanthanum carbonate were gastrointestinal events, such as nausea, vomiting, and abdominal pain and they generally abated over time with continued dosing.
In double-blind, placebo-controlled studies where a total of 180 and 95 patients with ESRD were randomized to lanthanum carbonate chewable tablet and placebo, respectively, for 4 to 6 weeks of treatment, the most common reactions that were more frequent (≥5% difference) in the lanthanum carbonate group were nausea, vomiting, and abdominal pain (Table 1).
| LANTHANUM CARBONATE % (N=180) | Placebo % (N=95) | |
|---|---|---|
| Nausea | 11 | 5 |
| Vomiting | 9 | 4 |
| Abdominal Pain | 5 | 0 |
* Expressed as the event rate for each term
In an open-label, long-term 2- year extension study in 93 patients who had transitioned from other studies, resulting in a total of up to 6 years treatment, mean baseline values and changes in transaminases were similar to those observed in the earlier comparative studies, with little change during treatment.
The safety of lanthanum carbonate was studied in two long-term, open-label clinical trials, which included 1,215 patients treated with lanthanum carbonate and 944 with alternative therapy. Fourteen percent (14%) of patients treated with lanthanum carbonate discontinued treatment due to adverse events. Gastrointestinal adverse reactions, such as nausea, diarrhea, and vomiting were the most common types of event leading to discontinuation.
In pooled active comparator controlled clinical trials, hypocalcemia was noted with an incidence of approximately 5% in both lanthanum and active comparator groups. A nonclinical study and a phase 1 study have shown reduced absorption of calcium in the intestine with lanthanum carbonate treatment.
In a crossover study in 72 healthy individuals comparing lanthanum carbonate chewable tablets to lanthanum carbonate oral powder, gastrointestinal adverse reactions such as nausea, diarrhea and vomiting were more common for the oral powder formulation (18%) than for the chewable tablets (7%).
The following adverse reactions have been identified during post-approval use of lanthanum carbonate. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Cases of constipation, intestinal perforation, intestinal obstruction, ileus, subileus, dyspepsia, allergic skin reactions, hypophosphatemia, and tooth injury while chewing the tablet have been reported.
There is a potential for lanthanum carbonate to interact with compounds which bind to cationic antacids (i.e., aluminum-, magnesium-, or calcium-based); therefore, do not administer such compounds within 2 hours of dosing with lanthanum carbonate. Examples of relevant classes of compounds where antacids have been demonstrated to reduce bioavailability include antibiotics (such as quinolones, ampicillin, and tetracyclines), thyroid hormones, ACE inhibitors, statin lipid regulators, and anti-malarials.
Co-administration of lanthanum carbonate with quinolone antibiotics may reduce the extent of their absorption. The bioavailability of oral ciprofloxacin was decreased by approximately 50% when taken with lanthanum carbonate in a single-dose study in healthy volunteers. Administer oral quinolone antibiotics at least 1 hour before or 4 hours after lanthanum carbonate. When oral quinolones are given for short courses, consider eliminating the doses of lanthanum carbonate that would normally be scheduled near the time of quinolone intake to improve quinolone absorption [see Clinical Pharmacology (12.3)].
The bioavailability of levothyroxine was decreased by approximately 40% when taken together with lanthanum carbonate. Administer thyroid hormone replacement therapy at least 2 hours before or 2 hours after dosing with lanthanum carbonate and monitor thyroid stimulating hormone (TSH) levels [see Clinical Pharmacology (12.3)].
There are no empirical data on avoiding drug interactions between lanthanum carbonate and most concomitant oral drugs. For oral medications where a reduction in the bioavailability of that medication would have a clinically significant effect on its safety or efficacy, consider separation of the timing of the administration of the two drugs. The duration of separation depends upon the absorption characteristics of the medication concomitantly administered, such as the time to reach peak systemic levels and whether the drug is an immediate-release or an extended-release product. Consider monitoring clinical responses or blood levels of concomitant medications that have a narrow therapeutic range.
Risk Summary
Available data from case reports with use of lanthanum carbonate in pregnant women are insufficient to identify a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. In animal reproduction studies, oral administration of lanthanum carbonate to pregnant rats and rabbits during organogenesis at doses 3 and 2.5 times, respectively, the maximum recommended human dose (MRHD), resulted in no adverse developmental effects. In rabbits, lanthanum carbonate doses 5 times the MRHD was associated with maternal toxicity and resulted in increased post-implantation loss, reduced fetal weights, and delayed fetal ossification (see Data). Deposition of lanthanum into developing bone, including growth plate, was observed in juvenile animals in long-term animal studies with lanthanum carbonate [see Use in Specific Populations (8.4)]. Use a non-lanthanum containing phosphate binder in a pregnant woman.
The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defect and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.
Data
Animal Data
In pregnant rats, oral administration of lanthanum carbonate at doses as high as 2,000 mg/kg/day during organogenesis resulted in no evidence of harm to the fetus. The MRHD for lanthanum carbonate is 5,725 mg, representing a dose of 95.4 mg/kg, or 3,530 mg/m2 for a 60-kg patient. The 2,000-mg/kg/day dose in the rat is equivalent to 12,000 mg/m2, 3 times the MRHD. In pregnant rabbits, oral administration of lanthanum carbonate at 1,500 mg/kg/day (18,000 mg/m2; 5 times the daily MRHD) during organogenesis was associated with increased post implantation loss, reduced fetal weights, and delayed fetal ossification. No effects on the pregnant rabbits or fetuses were observed at 750 mg/kg/day (9,000 mg/m2; 2.5 times the MRHD).
In a pre-and postnatal development study in the rat, pregnant rats were dosed at up to 2,000 mg/kg/day (12,000 mg/m2/day; equivalent to 3 times the MRHD) from day 6 of pregnancy through 20 days postpartum (including lactation). At 2,000 mg/kg/day, no maternal toxicity was observed, nor were any changes seen with respect to gestational length or delivery; however, piloerection/pallor, delayed eye opening, decreased body weight, and delayed sexual development were observed in the offspring at 2,000 mg/kg/day. At 200 and 600 mg/kg/day (equivalent to 0.3 and 1 time the MRHD, respectively), slight delays in sexual development (delayed vaginal opening) were observed in the female offspring [see Nonclinical Toxicology (13.2)].
Risk Summary
There are no data on the presence of lanthanum carbonate from lanthanum carbonate chewable tablet in human milk, the effects on the breastfed infant, or the effects on milk production. Deposition of lanthanum into developing bone, including growth plate, was observed in juvenile animals in long-term animal studies with lanthanum carbonate [see Use in Specific Populations (8.4)]. Use a non-lanthanum containing phosphate binder in a lactating woman.
The safety and efficacy of lanthanum carbonate in pediatric patients have not been established. While growth abnormalities were not identified in long-term animal studies, lanthanum was deposited into developing bone, including growth plate. The consequences of such deposition in developing bone in pediatric patients are unknown; therefore, the use of lanthanum carbonate in this population is not recommended.
Of the total number of patients in clinical studies of lanthanum carbonate, 32% (538) were ≥65 years of age, while 9.3% (159) were ≥75 years of age. No overall differences in safety or effectiveness were observed between patients ≥65 years of age and younger patients.
The symptoms associated with overdose are adverse reactions such as headache, nausea and vomiting. In clinical trials in healthy adults, gastrointestinal (GI) symptoms were reported with daily doses up to 6,000 mg/day of lanthanum carbonate administered with food. Given the topical activity of lanthanum in the gut, and the excretion of the majority of the dose in feces, supportive therapy is recommended for overdosage. Lanthanum carbonate was not acutely toxic in animals by the oral route. No deaths and no adverse effects occurred in mice, rats, or dogs after single oral doses of 2,000 mg/kg (1.7, 3.4, and 11.3 times the MRHD, respectively, on a mg/m2 basis).
Lanthanum carbonate chewable tablets contains lanthanum carbonate with molecular formula La2(CO3)3 and molecular weight 457.8 (anhydrous mass). Lanthanum carbonate is described as white to almost-white powder. Lanthanum carbonate is practically insoluble in water and is insoluble in organic solvents; it dissolves in dilute mineral acids with effervescence.
Each lanthanum carbonate chewable tablet, off-white to yellowish, chewable tablet contains lanthanum carbonate equivalent to 500, 750, or 1,000 mg of elemental lanthanum and the following inactive ingredients: microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose, dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
Lanthanum carbonate is a phosphate binder that reduces absorption of phosphate by forming insoluble lanthanum phosphate complexes that pass through the GI tract unabsorbed. Both serum phosphate and calcium phosphate product are reduced as a consequence of the reduced dietary phosphate absorption.
In vitro studies have shown that lanthanum binds phosphate in the physiologically relevant pH range of 3 to 7. In simulated gastric fluid, lanthanum binds approximately 97% of the available phosphate at pH 3-5 and 67% at pH 7, when lanthanum is present in a two-fold molar excess to phosphate. Bile acids have not been shown to affect the phosphate binding affinity of lanthanum. In order to bind dietary phosphate, lanthanum carbonate chewable tablets must be administered with or immediately after meals.
In five phase 1 pharmacodynamic studies comparing the reduction from baseline of urinary phosphorus excretion in healthy volunteers (N=143 taking lanthanum carbonate), it was shown that the mean intestinal phosphate binding capacity of lanthanum ranged from 235 to 468 mg phosphorus/day when lanthanum was administered at a dose of 3 g per day with food. By comparison, in one study with an untreated control group (n=10) and another study with a placebo group (n=3), the corresponding mean changes from baseline were 3 mg phosphorus/day and 87 mg phosphorus/day, respectively.
In healthy subjects, lanthanum carbonate oral powder and lanthanum carbonate chewable tablets produce similar effects on urinary phosphate excretion.
Absorption and Distribution - Following single- or multiple- dose oral administration of lanthanum carbonate to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%). Following oral administration in patients, the mean lanthanum Cmax was 1.0 ng/mL. During long-term administration (52 weeks) in patients with ESRD , the mean lanthanum concentration in plasma was approximately 0.6 ng/mL. There was a minimal increase in plasma lanthanum concentrations with increasing doses within the therapeutic dose range. The timing of food intake relative to lanthanum administration (during and 30 minutes after food intake) has a negligible effect on the systemic level of lanthanum.
Systemic exposure to lanthanum was approximately 30% higher following administration of Lanthanum Carbonate Oral Powder when compared to Lanthanum Carbonate Chewable Tablets. However, systemic exposure to lanthanum from both formulations in this study was within the range seen in previous pharmacokinetic studies of Chewable Tablets in healthy individuals.
In vitro, lanthanum is highly bound (>99%) to human plasma proteins, including human serum albumin, α1-acid glycoprotein, and transferrin. Binding to erythrocytes in vivo is negligible in rats.
In animal studies, lanthanum concentrations in several tissues, particularly gastrointestinal tract, mesenteric lymph nodes, bone, and liver, increased over time to levels several orders of magnitude higher than those in plasma. The level of lanthanum in the liver was higher in renally impaired rats due to higher intestinal absorption. Lanthanum was found in the lysosomes and the biliary canal consistent with transcellular transport. Steady state tissue concentrations in bone and liver were achieved in dogs between 4 and 26 weeks. Relatively high levels of lanthanum remained in these tissues for longer than 6 months after cessation of dosing in dogs. There is no evidence from animal studies that lanthanum crosses the blood-brain barrier. In 105 bone biopsies from patients treated with lanthanum carbonate for up to 4.5 years, rising levels of lanthanum were noted over time. Estimates of elimination half-life from bone ranged from 2.0 to 3.6 years. Steady state bone concentrations were not reached during the period studied.
Metabolism and Elimination - Lanthanum is not metabolized. Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
No information is available regarding the mass balance of lanthanum in humans after oral administration. In rats and dogs, the mean recovery of lanthanum after an oral dose was about 99% and 94%, respectively, and was essentially all from feces. Biliary excretion is the predominant route of elimination for circulating lanthanum in rats. In healthy volunteers administered intravenous (IV) lanthanum as the soluble chloride salt (120 mcg), renal clearance was less than 2% of total plasma clearance.
Drug Interactions
Lanthanum carbonate has a low potential for systemic drug-drug interactions because of the very low bioavailability of lanthanum and because it is not a substrate or inhibitor of major cytochrome P450 enzyme groups involved in drug metabolism (CYP1A2, CYP2C9/10, CYP2C19, CYP2D6,and CYP3A4/5).
Lanthanum carbonate does not alter gastric pH; herefore, lanthanum carbonate drug interactions based on altered gastric pH are not expected.
In an in vitro investigation, lanthanum did not form insoluble complexes when mixed in simulated gastric fluid with warfarin, digoxin, furosemide, phenytoin, metoprolol, and enalapril. Clinical studies have shown that lanthanum carbonate (three doses of 1,000 mg on the day prior to exposure and one dose of 1,000 mg on the day of co-administration) administered 30 minutes earlier did not alter the pharmacokinetics of oral warfarin (10 mg), digoxin (0.5 mg), or metoprolol (100 mg). Potential pharmacodynamic interactions between lanthanum and these drugs (e.g., bleeding time or prothrombin time) were not evaluated. None of the drug interaction studies were done with the maximum recommended therapeutic dose of lanthanum carbonate. No drug interaction studies assessed the effects of drugs on phosphate binding by lanthanum carbonate.
Ciprofloxacin
In a randomized, two–way crossover study in healthy volunteers examining the interaction potential of a single oral dose of ciprofloxacin (750 mg) alone and with lanthanum carbonate (1 g three times a day), the maximum plasma concentration of ciprofloxacin was reduced by 56% and the area under the ciprofloxacin plasma concentration-time curve was reduced by 54%. The 24-hour urinary recovery of ciprofloxacin was reduced 52% by lanthanum carbonate [see Drug Interactions (7.2)].
Levothyroxine
In a single-dose crossover study of levothyroxine (1 mg) with or without simultaneous administration of a single dose of lanthanum carbonate (500 mg) in six euthyroid normal healthy volunteers, the area under the serum T4 concentration-time curve was decreased by 40% [see Drug Interactions (7.3)].
Fat -Soluble Vitamins
Lanthanum carbonate chewable tablets appears not to affect the availability of fat- soluble vitamins (A, D, E, and K) or other nutrients [see Clinical Studies (14.2)].
Citrate
Citrate did not increase the absorption of lanthanum.
Oral administration of lanthanum carbonate to rats for up to 104 weeks, at doses up to 1,500 mg of the salt per kg/day (2.5 times the MRHD of 5,725 mg, on a mg/m2 basis, assuming a 60-kg patient) revealed no evidence of carcinogenic potential. In the mouse, oral administration of lanthanum carbonate for up to 99 weeks, at a dose of 1,500 mg/kg/day (1.3 times the MRHD) was associated with an increased incidence of glandular stomach adenomas in male mice.
Lanthanum carbonate tested negative for mutagenic activity in an in vitro Ames assay using Salmonella typhimurium and Escherichia coli strains and in vitro HGPRT gene mutation and chromosomal aberration assays in Chinese hamster ovary cells. Lanthanum carbonate also tested negative in an oral mouse micronucleus assay at doses up to 2,000 mg/kg (1.7 times the MRHD), and in micronucleus and unscheduled DNA synthesis assays in rats given IV lanthanum chloride at doses up to 0.1 mg/kg, a dose that produced plasma lanthanum concentrations greater than 2,000 times the peak human plasma concentration.
Lanthanum carbonate, at doses up to 2,000 mg/kg/day (3.4 times the MRHD), did not affect fertility or mating performance of male or female rats.
In pregnant rats, oral administration of lanthanum carbonate at doses as high as 2,000 mg/kg/day (3.4 times the MRHD) resulted in no evidence of harm to the fetus. In pregnant rabbits, oral administration of lanthanum carbonate at 1,500 mg/kg/day (5 times the MRHD) was associated with a reduction in maternal body weight gain and food consumption, increased post-implantation loss, reduced fetal weights, and delayed fetal ossification. No effects on pregnant rabbits or fetuses were observed at 750 mg/kg/day (2.5 times the MRHD). Lanthanum carbonate administered to rats from implantation through lactation at 2,000 mg/kg/day (3.4 times the MRHD) caused delayed eye opening, reduction in body weight gain, and delayed sexual development (preputial separation and vaginal opening) of the offspring. At 200 and 600 mg/kg/day (equivalent to 0.3 and 1 time the MRHD, respectively), slight delays in vaginal opening were observed in the female offspring.
The effectiveness of lanthanum carbonate in reducing serum phosphorus in patients with ESRD was demonstrated in one short-term, placebo-controlled, double-blind dose-ranging study; two placebo-controlled randomized withdrawal studies; and two long-term, active-controlled, open-label studies in patients undergoing either hemodialysis or peritoneal dialysis.
One -hundred and forty-four patients with chronic renal failure undergoing hemodialysis and with elevated phosphate levels were randomized to double-blind treatment at a fixed dose of lanthanum carbonate of 225 mg (n=27), 675 mg (n=29), 1,350 mg (n=30) or 2,250 mg (n=26) or placebo (n=32) in divided doses with meals. Fifty-five percent of subjects were male, 71% black, 25% white, and 4% of other races. The mean age was 56 years and the duration of dialysis ranged from 0.5 to 15.3 years. Steady-state effects were achieved after two weeks. The effect after six weeks of treatment is shown in Figure 1.
Figure 1. Difference in Phosphate Reduction in the Lanthanum Carbonate and Placebo Group in a 6-Week, Dose- Ranging, Double-Blind Study in Patients with ESRD (with 95% Confidence Intervals)
One-hundred and eighty-five patients with ESRD undergoing either hemodialysis (n=146) or peritoneal dialysis (n=39) were enrolled in two placebo-controlled, randomized withdrawal studies. Sixty-four percent of subjects were male, 28% black, 62% white, and 10% of other races. The mean age was 58.4 years and the duration of dialysis ranged from 0.2 to 21.4 years. After titration of lanthanum carbonate to achieve a phosphate level between 4.0 and 5.6 mg/dL in one study (doses up to 2,250 mg/day) or ≤5.9 mg/dL in the second study (doses up to 3,000 mg/day) and maintenance through 6 weeks, patients were randomized to lanthanum or placebo. During the placebo-controlled, randomized withdrawal phase (four weeks), the phosphorus concentration rose in the placebo group by 1.7 mg/dL in one study and 1.9 mg/dL in the other study relative to patients who remained on lanthanum carbonate therapy.
Two long-term open-label studies were conducted, involving a total of 2,028 patients with ESRD undergoing hemodialysis. Patients were randomized to receive lanthanum carbonate or alternative phosphate binders for up to six months in one study and two years in the other. The daily lanthanum carbonate chewable tablets doses; divided and taken with meals, ranged from 375 mg to 3,000 mg. Doses were titrated to reduce serum phosphate levels to a target level. The daily doses of the alternative therapy were based on current prescribing information or those commonly utilized. Both treatment groups had similar reductions in serum phosphate of about 1.8 mg/dL. Maintenance of reduction was observed for up to three years in patients treated with lanthanum carbonate in long-term, open-label extensions.
No effects of lanthanum carbonate on serum levels of 25-dihydroxy vitamin D3, vitamin A, vitamin B12, vitamin E, and vitamin K were observed in patients who were monitored for 6 months.
Paired bone biopsies (at baseline and at one or two years) in 69 patients randomized to either lanthanum carbonate or calcium carbonate in one study and 99 patients randomized to either lanthanum carbonate or alternative therapy in a second study showed no differences in the development of mineralization defects between the groups.
Vital status was known for over 2,000 patients, 97% of those participating in the clinical program during and after receiving treatment. The adjusted yearly mortality rate (rate/years of observation) for patients treated with lanthanum carbonate chewable tablets or alternative therapy was 6.6%.
Lanthanum carbonate is supplied as chewable tablets in three dosage strengths for oral administration: 500-mg tablets, 750-mg tablets, and 1000-mg tablets.
Each 500-mg chewable tablet is off-white to yellowish white, round flat faced bevel edge debossed “IG” on one side with “476” on the other.
500- mg Patient Pack (2 bottles of 45 tablets, NDC 69097-934-57, per each patient pack) NDC 69097-934-98
Each 750-mg chewable tablet is off-white to yellowish white, round flat faced bevel edge debossed “IG” on one side with “477” on the other.
750-mg Patient Pack (6 bottles of 15 tablets, NDC 69097-935-89, per each patient pack) NDC 69097-935-98
Each 1000-mg chewable tablet is off-white to yellowish white, round flat faced bevel edge debossed “IG” on one side with “478” on the other.
1000-mg Patient Pack (9 bottles of 10 tablets, NDC 69097-936-65, per each patient pack) NDC 69097-936-98
Storage and Handling
Store Lanthanum Carbonate Chewable Tablets at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Revised:08/2024
| MEDICATION GUIDE LANTHANUM CARBONATE CHEWABLE TABLETS (LAN-tha-num KAR-bo-nate) |
Read this Medication Guide before you start taking lanthanum carbonate chewable tablets and each time you get a refill. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or treatment.
What is the most important information I should know about lanthanum carbonate chewable tablets?
Lanthanum carbonate chewable tablets may cause a bowel blockage, a hole in the bowel, or severe constipation, which can be serious, and sometimes lead to surgery or treatment in a hospital.
Do not swallow lanthanum carbonate chewable tablets whole. Chew tablets completely before swallowing. If you cannot chew tablets completely, you may crush the tablets thoroughly before swallowing or discuss the oral powder formulation with your healthcare provider.
What are lanthanum carbonate chewable tablets?
Lanthanum carbonate chewable tablets are a prescription medicine used in people with end- stage renal disease (ESRD) to lower the amount of phosphate in the blood.
Who should not take lanthanum carbonate chewable tablets?
Do not take lanthanum carbonate chewable tablets if you:
Lanthanum carbonate chewable tablets have not been studied in children and adolescents under 18 years of age.
What should I tell my healthcare provider before taking lanthanum carbonate chewable tablets?
Lanthanum carbonate chewable tablets may not be right for you. Before starting lanthanum carbonate chewable tablets, tell your healthcare provider if you:
Especially tell your healthcare provider if you take:
Know the medicines you take. Keep a list of them and show it to your healthcare provider and pharmacist when you get a new medicine.
How should I take lanthanum carbonate chewable tablets?
What are possible or reasonably likely side effects of lanthanum carbonate chewable tablets?
See “What is the most important information I should know about lanthanum carbonate chewable tablets?”
The most common side effects of lanthanum carbonate chewable tablets include:
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the side effects of lanthanum carbonate chewable tablets. For more information, ask your healthcare provider or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
How should I store lanthanum carbonate chewable tablets?
Keep lanthanum carbonate chewable tablets and all medicines out of the reach of children.
General information about lanthanum carbonate chewable tablets
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use lanthanum carbonate chewable tablets for a condition for which it was not prescribed. Do not give lanthanum carbonate chewable tablets to other people, even if they have the same condition. It may harm them.
This Medication Guide summarizes the most important information about lanthanum carbonate chewable tablets. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information about lanthanum carbonate chewable tablets that is written for healthcare professionals.
For more information call Cipla Ltd. at 1-866-604-3268
What are the ingredients in lanthanum carbonate chewable tablets?
Active ingredient: lanthanum carbonate
Inactive ingredients: microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose, dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
This Medication Guide has been approved by the US Food and Drug Administration.
Manufactured by:
InvaGen Pharmaceuticals, Inc.
(a subsidiary of Cipla Ltd.)
Hauppauge, NY 11788
or
Manufactured by:
Genvion Corporation
500 Camiel Sys Street
Winnipeg, MB Canada R2J 4K2
Manufactured for:
Cipla USA, Inc.
10 Independence Boulevard, Suite 300
Warren, NJ 07059
08/2024
| SAP-21106205-08-2024 |
NDC 69097-934-98
Rx Only
Lanthanum Carbonate
chewable tablets
500 mg*
Do not swallow tablets whole. Chew or crush tablets completely
before swallowing. Take with or immediately after meals.
PHARMACIST: Dispense the Medication
Guide provided seperately to each patient.
*Active Ingredient:
Each tablet contains 500 mg of lanthanum as lanthanum carbonate anhydrous.
Inactive Ingredients:
Microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose,
dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
See package insert for full prescribing information.
Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
2 bottles/45 chewable tablets each
Cipla
NDC 69097-935-98
Rx Only
Lanthanum Carbonate
chewable tablets
750 mg*
Do not swallow tablets whole. Chew or crush tablets completely
before swallowing. Take with or immediately after meals.
PHARMACIST: Dispense the Medication
Guide provided seperately to each patient.
*Active Ingredient:
Each tablet contains 750 mg of lanthanum as lanthanum carbonate anhydrous.
Inactive Ingredients:
Microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose,
dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
See package insert for full prescribing information.
Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
6 bottles/15 chewable tablets each
Cipla
NDC 69097-936-98
Rx Only
Lanthanum Carbonate
chewable tablets
1000 mg*
Do not swallow tablets whole. Chew or crush tablets completely
before swallowing. Take with or immediately after meals.
PHARMACIST: Dispense the Medication
Guide provided seperately to each patient.
*Active Ingredient:
Each tablet contains 1000 mg of lanthanum as lanthanum carbonate anhydrous.
Inactive Ingredients:
Microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose,
dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
See package insert for full prescribing information.
Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
9 bottles/10 chewable tablets each
Cipla
NDC 69097-934-57
Lanthanum Carbonate Tablets, 500 mg
45 Tablets
Rx only
NDC 69097-935-89
Lanthanum Carbonate Tablets, 750 mg
15 Tablets
Rx only
NDC 69097-936-65
Lanthanum Carbonate Tablets, 1000 mg
10 Tablets
Rx only
NDC 69097-934-98
Rx Only
Lanthanum Carbonate
chewable tablets
500 mg*
Do not swallow tablets whole. Chew or crush tablets completely
before swallowing. Take with or immediately after meals.
PHARMACIST: Dispense the Medication
Guide provided seperately to each patient.
*Active Ingredient:
Each tablet contains 500 mg of lanthanum as lanthanum carbonate anhydrous.
Inactive Ingredients:
Microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose,
dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
See package insert for full prescribing information.
Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
2 bottles/45 chewable tablets each
Cipla
NDC 69097-935-98
Rx Only
Lanthanum Carbonate
chewable tablets
750 mg*
Do not swallow tablets whole. Chew or crush tablets completely
before swallowing. Take with or immediately after meals.
PHARMACIST: Dispense the Medication
Guide provided seperately to each patient.
*Active Ingredient:
Each tablet contains 750 mg of lanthanum as lanthanum carbonate anhydrous.
Inactive Ingredients:
Microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose,
dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
See package insert for full prescribing information.
Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
6 bottles/15 chewable tablets each
Cipla
NDC 69097-936-98
Rx Only
Lanthanum Carbonate
chewable tablets
1000 mg*
Do not swallow tablets whole. Chew or crush tablets completely
before swallowing. Take with or immediately after meals.
PHARMACIST: Dispense the Medication
Guide provided seperately to each patient.
*Active Ingredient:
Each tablet contains 1000 mg of lanthanum as lanthanum carbonate anhydrous.
Inactive Ingredients:
Microcrystalline cellulose, guar gum, sucralose, hydroxypropyl cellulose,
dextrates, colloidal silicon dioxide, stearic acid, magnesium stearate.
See package insert for full prescribing information.
Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]
9 bottles/10 chewable tablets each
Cipla
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 602635 | lanthanum carbonate 1000 MG Chewable Tablet | PSN | 4 |
| 477347 | lanthanum carbonate 500 MG Chewable Tablet | PSN | 4 |
| 642452 | lanthanum carbonate 750 MG Chewable Tablet | PSN | 4 |
| 602635 | lanthanum carbonate 1000 MG Chewable Tablet | SCD | 4 |
| 477347 | lanthanum carbonate 500 MG Chewable Tablet | SCD | 4 |
| 642452 | lanthanum carbonate 750 MG Chewable Tablet | SCD | 4 |
| Class | Version | Type | Effective |
|---|---|---|---|
| LANTHANUM CATION (3+) Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| cd999b70-ef95-1812-9f06-f589ecff7593 | Product name | 5 | 20251216 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69097-934-57 | Lanthanum carbonate | 45 in 1 BOTTLE | TABLET, CHEWABLE | 45 | 4 | |
| 69097-934-98 | Lanthanum carbonate | 2 in 1 PACKAGE | TABLET, CHEWABLE | 2 | 4 | |
| 69097-935-89 | Lanthanum carbonate | 15 in 1 BOTTLE | TABLET, CHEWABLE | 15 | 4 | |
| 69097-935-98 | Lanthanum carbonate | 6 in 1 PACKAGE | TABLET, CHEWABLE | 6 | 4 | |
| 69097-936-65 | Lanthanum carbonate | 10 in 1 BOTTLE | TABLET, CHEWABLE | 10 | 4 | |
| 69097-936-98 | Lanthanum carbonate | 9 in 1 PACKAGE | TABLET, CHEWABLE | 9 | 4 |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69097-934-57 | EA - Each | 69097-934 | 54fb4d71-0f66-4e3b-80c4-240309d0fed8 | 1 | 2022-03-09 |
| 69097-934-98 | EA - Each | 69097-934 | 1347f4cb-2665-4e32-b973-66faa22ac22c | 1 | 2022-03-09 |
| 69097-935-89 | EA - Each | 69097-935 | 54e6b48d-65ba-40e5-a880-4ad89e94edcb | 1 | 2022-03-09 |
| 69097-935-98 | EA - Each | 69097-935 | 88725373-7ece-4b27-b639-44aa85db9638 | 1 | 2022-03-09 |
| 69097-936-65 | EA - Each | 69097-936 | 5f13dca0-8ee3-4326-9a32-c81306c4a0b8 | 1 | 2022-03-09 |
| 69097-936-98 | EA - Each | 69097-936 | 238dad20-9ca1-4aee-97b8-10697a5a6dd8 | 1 | 2022-03-09 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 69097-934 | 69097-934-57, 69097-934-98 |
| 69097-935 | 69097-935-89, 69097-935-98 |
| 69097-936 | 69097-936-65, 69097-936-98 |
Every source-derived ingredient row is available through these pages.
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A206868-001 | LANTHANUM CARBONATE | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | |
| A206868-002 | LANTHANUM CARBONATE | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | |
| A206868-003 | LANTHANUM CARBONATE | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 |
| Application-product | TE code |
|---|---|
| A206868-001 | AB |
| A206868-002 | AB |
| A206868-003 | AB |
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 84e616aacf4f… | |
| 2026-09-14 22:38:34 | 2026-08 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | caaa826d4ba7… | |
| 2026-08-18 06:07:40 | 2026-07 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 011fe1cb6892… | |
| 2026-02-19 14:30 UTC | 2026-02 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 31067a03dcf5… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 6a471c1ec25d… | |
| 2025-08-23 18:47 UTC | 2025-08 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | fd3edfee7708… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | b8a1b40f171c… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 03ed91905a0d… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 03ed91905a0d… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 03ed91905a0d… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 2680178bc6a6… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 2680178bc6a6… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 2680178bc6a6… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 5bbf6a4d5a75… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 5bbf6a4d5a75… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 5bbf6a4d5a75… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | d8e5a09893c0… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | d8e5a09893c0… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | d8e5a09893c0… | |
| 2024-10-29 15:01 UTC | 2024-10 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | d06236e962d9… | |
| 2024-10-29 15:01 UTC | 2024-10 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | d06236e962d9… | |
| 2024-10-29 15:01 UTC | 2024-10 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | d06236e962d9… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 79d66fd596c7… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A206868-002 | LANTHANUM CARBONATE | EQ 750MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 79d66fd596c7… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A206868-003 | LANTHANUM CARBONATE | EQ 1GM BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 79d66fd596c7… | |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | A206868-001 | LANTHANUM CARBONATE | EQ 500MG BASE | TABLET, CHEWABLE / ORAL | AB | 2022-01-24 | 301d65b070ca… |
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | A206868-001 | AB | 1 | 84e616aacf4f… |
| 2026-09-14 22:38:34 | 2026-08 | A206868-002 | AB | 1 | 84e616aacf4f… |
| 2026-09-14 22:38:34 | 2026-08 | A206868-003 | AB | 1 | 84e616aacf4f… |
| 2026-08-18 06:07:40 | 2026-07 | A206868-001 | AB | 1 | caaa826d4ba7… |
| 2026-08-18 06:07:40 | 2026-07 | A206868-002 | AB | 1 | caaa826d4ba7… |
| 2026-08-18 06:07:40 | 2026-07 | A206868-003 | AB | 1 | caaa826d4ba7… |
| 2026-02-19 14:30 UTC | 2026-02 | A206868-001 | AB | 1 | 011fe1cb6892… |
| 2026-02-19 14:30 UTC | 2026-02 | A206868-002 | AB | 1 | 011fe1cb6892… |
| 2026-02-19 14:30 UTC | 2026-02 | A206868-003 | AB | 1 | 011fe1cb6892… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A206868-001 | AB | 1 | 31067a03dcf5… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A206868-002 | AB | 1 | 31067a03dcf5… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | A206868-003 | AB | 1 | 31067a03dcf5… |
| 2025-08-23 18:47 UTC | 2025-08 | A206868-001 | AB | 1 | 6a471c1ec25d… |
| 2025-08-23 18:47 UTC | 2025-08 | A206868-002 | AB | 1 | 6a471c1ec25d… |
| 2025-08-23 18:47 UTC | 2025-08 | A206868-003 | AB | 1 | 6a471c1ec25d… |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A206868-001 | AB | 1 | fd3edfee7708… |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A206868-002 | AB | 1 | fd3edfee7708… |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | A206868-003 | AB | 1 | fd3edfee7708… |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A206868-001 | AB | 1 | b8a1b40f171c… |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A206868-002 | AB | 1 | b8a1b40f171c… |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | A206868-003 | AB | 1 | b8a1b40f171c… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A206868-001 | AB | 1 | 03ed91905a0d… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A206868-002 | AB | 1 | 03ed91905a0d… |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | A206868-003 | AB | 1 | 03ed91905a0d… |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A206868-001 | AB | 1 | 2680178bc6a6… |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A206868-002 | AB | 1 | 2680178bc6a6… |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | A206868-003 | AB | 1 | 2680178bc6a6… |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A206868-001 | AB | 1 | 5bbf6a4d5a75… |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A206868-002 | AB | 1 | 5bbf6a4d5a75… |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | A206868-003 | AB | 1 | 5bbf6a4d5a75… |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A206868-001 | AB | 1 | d8e5a09893c0… |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A206868-002 | AB | 1 | d8e5a09893c0… |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | A206868-003 | AB | 1 | d8e5a09893c0… |
| 2024-10-29 15:01 UTC | 2024-10 | A206868-001 | AB | 1 | d06236e962d9… |
| 2024-10-29 15:01 UTC | 2024-10 | A206868-002 | AB | 1 | d06236e962d9… |
| 2024-10-29 15:01 UTC | 2024-10 | A206868-003 | AB | 1 | d06236e962d9… |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A206868-001 | AB | 1 | 79d66fd596c7… |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A206868-002 | AB | 1 | 79d66fd596c7… |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | A206868-003 | AB | 1 | 79d66fd596c7… |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | A206868-001 | AB | 1 | 301d65b070ca… |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lanthanum carbonate | LANTHANUM CARBONATE | Cipla USA Inc. | 1d5ff930-1189-4e96-bdfb-9fd9c2c83d1b | 2024-08-01 | Warnings, Adverse reactions | 69097-935-89 69097-934-98 69097-935-98 69097-936-98 69097-934-57 69097-936-65 69097-936 69097-935 69097-934 69097093589 69097093498 69097093598 69097093698 69097093457 69097093665 df0330c5-d556-4698-accd-70a9c948687d 1d5ff930-1189-4e96-bdfb-9fd9c2c83d1b |
Adverse event summaries are temporarily unavailable. Other product information remains available.