AMPICILLIN CAPSULES, USP 500 mg Rx Only

Manufacturer
H.J. Harkins Company, Inc. | DAVA Pharmaceuticals, Inc. | STADA Production Ireland, Ltd. | Sandoz Industrial Products S.A | Antibioticos, SA
Effective date
2012-08-28
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:15:41

Label at a glance#

ProductAmpicillin
Active ingredientAMPICILLIN TRIHYDRATE
Label structure12 sections

Indications and uses

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ampicillin capsules, Ampicillin for Oral Suspension and other antibacterial drugs, Ampicillin capsules and Ampicillin for Oral Suspension should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.  When culture and susceptibility information are available, they should be co...

Dosage and administration

Adults and children weighing over 20 Kg: For genitourinary or gastrointestinal tract infections other than gonorrhea in men and women , the usual dose is 500 mg q.i.d. in equally spaced doses; severe or chronic infections may require larger doses. For the treatment of gonorrhea in both men and women, a single oral dose of 3.5 grams of ampicillin administered simultaneously with 1 gram of probenecid is recommended....

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ampicillin capsules, Ampicillin for Oral Suspension and other antibacterial drugs, Ampicillin Capsules and Ampicillin for Oral Suspension should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.

DESCRIPTION

DESCRIPTION SECTION

Ampicillin trihydrate is a semisynthetic penicillin derived from the basic penicillin nucleus, 6-aminopenicillanic acid. Ampicillin is designated chemically as (2S, 5R, 6R)-6-[(R)-2-Amino-2-phenylacetamido]-3, 3-dimethyl-7-oxo-4-thia-l-azabicyclo[3.2.0]heptane-2-carboxylic acid trihydrate.

It has the following chemical structure:

Ampicillin trihydrate Chemical Structure
Ampicillin trihydrate Chemical Structure

The molecular formula is C16H19N3O4S.3H2O, and the molecular weight is 403.45.

Ampicillin Capsules, USP for oral administration provide ampicillin trihydrate equivalent to 250 mg and 500 mg ampicillin. Ampicillin Capsules, USP also contains magnesium stearate, NF. The capsule shell contains black iron oxide; D&C red No. 28; FD&C blue No. 1; gelatin, NF; silicon dioxide, NF; sodium lauryl sulfate, NF; titanium dioxide USP.

Ampicillin for Oral Suspension, USP provides ampicillin trihydrate equivalent to 125 mg/5 mL and 250 mg/5 mL ampicillin. Ampicillin for Oral Suspension, USP also contains flavors; microcrystalline cellulose and carboxymethylcellulose sodium, NF; colloidal silicon dioxide, NF; sodium citrate, USP; sodium propionate, NF; sucrose, NF

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Ampicillin is bactericidal at low concentrations and is clinically effective not only against the gram-positive organisms usually susceptible to penicillin G but also against a variety of gram-negative organisms. It is stable in the presence of gastric acid and is well absorbed from the gastrointestinal tract. It diffuses readily into most body tissues and fluids; however, penetration into the cerebrospinal fluid and brain occurs only with meningeal inflammation. Ampicillin is excreted largely unchanged in the urine; its excretion can be delayed by concurrent administration of probenecid which inhibits the renal tubular secretion of ampicillin. In blood serum, ampicillin is the least bound of all the penicillins; an average of about 20 percent of the drug is bound to the plasma proteins as compared to 60 to 90 percent of the other penicillins. The administration of 500 mg dose of ampicillin trihydrate capsules results in an average peak blood serum level of approximately 3.0 mcg/mL; the average peak serum level for a 250 mg dose of ampicillin trihydrate for oral suspension is approximately 2.3 mcg/mL.

Microbiology: While in vitro studies have demonstrated the susceptibility of most strains of the following organisms, clinical efficacy for infections other than those included in the INDICATIONS AND USAGE section has not been documented.

GRAM-POSITIVE - strains of alpha- and beta-hemolytic streptococci, Streptococcus pneumoniae, those strains of staphylococci, which do not produce penicillinase, Clostridium sp., Bacillus anthracis , Corynebacterium xerose, and most strains of enteracocci.

GRAM-NEGATIVE – Hemophilus influenzae ; Neisseria gonorrhoeae and N. Meningitidis , Proteus mirabilis and many strains of Salmonella (including S. typhosa), Shigella and Escherichia coli.

NOTE: Ampicillin is inactivated by penicillinase and therefore is ineffective against penicillinase-producing organisms including certain strains at staphylococci, Pseudomonas aeruginosa, P. vulgaris, Klebsiella pneumoniae , Enterobacter aerogenes, and some strains of E. coli. Ampicillin is not active against Rickettsia, Mycoplasma, and "large viruses" (Miyagawanella).

TESTING FOR SUSCEPTIBILITY: The invading organism should be cultured and its susceptibility demonstrated as a guide to therapy. If the Kirby-Bauer method of disc susceptibility is used, a 10 mcg ampicillin disc should be used to determine the relative in vitro susceptibility.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ampicillin capsules, Ampicillin for Oral Suspension and other antibacterial drugs, Ampicillin capsules and Ampicillin for Oral Suspension should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria.  When culture and susceptibility information are available, they should be considered in selecting of modifying anitimicrobial therapy, in the absence of such data, local epidemiology and susceptibility patterns contribute to the empiric selection of therapy.

Ampicillin capsules and Ampicillin for oral suspension are indicated in the treatment of infections caused by susceptible strains of the designated organisms listed below:

Infections of the genitourinary tract including gonorrhea - E. coli, P. mirabilis, enterococci, Shigella , S. typhosa and other Salmonella and nonpenicillinase-producing N. gonorrhoeae.

Infections of the respiratory tract - Nonpenicillinase-producing H. influenzae and staphylococci, and streptococci including Streptococcus pneumoniae.

Infections of the gastrointestinal tract - Shigella , S. typhosa and other Salmonella, E. coli, P. mirabilis, and enterococci.

Meningitis - N. Meningitidis

Bacteriology studies to determine the causative organisms and their susceptibility to ampicillin should be performed. Therapy may be instituted prior to the results of susceptibility testing.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

A history of a previous hypersensitivity reaction to any of the penicillins is a contraindication. Ampicillin is also contraindicated in infections caused by penicillinase-producing organisms.

WARNINGS

WARNINGS SECTION

SERIOUS AND OCCASIONALLY FATAL HYPERSENSITIVITY (ANAPHYLACTOID) REACTIONS HAVE BEEN REPORTED IN PATIENTS ON PENICILLIN THERAPY. ALTHOUGH ANAPHYLAXIS IS MORE FREQUENT FOLLOWING PARENTERAL THERAPY, IT HAS OCCURRED IN PATIENTS ON ORAL PENICILLINS. THESE REACTIONS ARE MORE LIKELY TO OCCUR IN INDIVIDUALS WITH A HISTORY OF SENSITIVITY TO MULTIPLE ALLERGENS. THERE HAVE BEEN REPORTS OF INDIVIDUALS WITH A HISTORY OF PENICILLIN HYPERSENSITIVITY WHO HAVE EXPERIENCED SEVERE REACTIONS WHEN TREATED WITH CEPHALOSPORINS. BEFORE THERAPY WITH ANY PENICILLIN, CAREFUL INQUIRY SHOULD BE MADE CONCERNING PREVIOUS HYPERSENSITIVITY REACTIONS TO PENICILLINS, CEPHALOSPORINS, OR OTHER ALLERGENS. IF AN ALLERGIC REACTION OCCURS, APPROPRIATE THERAPY SHOULD BE CONSIDERED. SERIOUS ANAPHYLACTOID REACTIONS REQUIRE IMMEDIATE EMERGENCY TREATMENT WITH EPINEPHRINE. OXYGEN, INTRAVENOUS STEROIDS, AND AIRWAY MANAGEMENT, INCLUDING INTUBATION, SHOULD ALSO BE ADMINISTERED AS INDICATED.

Pseudomembranous colitis has been reported with nearly all antibacterial agents, including ampicillin, and may range in severity from mild to life-threatening. Therefore, it is important to consider this diagnosis in patients who present with diarrhea subsequent to the administration of antibacterial agents.

Treatment with antibacterial agents alters the normal flora of the colon and may permit overgrowth of clostridia. Studies indicate that a toxin produced by Clostridium difficile is a primary cause of "antibiotic-associated colitis".

After the diagnosis of pseudomembranous colitis has been established, therapeutic measures should be initiated. Mild cases of pseudomembranous colitis usually respond to discontinuation of the drug alone. In moderate to severe cases, consideration should be given to management with fluids and electrolytes, protein supplementation, and treatment with an antibacterial drug clinically effective against C. difficile colitis.

PRECAUTIONS

PRECAUTIONS SECTION

General

GENERAL PRECAUTIONS SECTION

Prescribing Ampicillin capsules and Ampicillin for Oral Suspension in the absence of a proven or strongly suspected bacterial infection of a prophylactic indication is unlikely to provide benefit to the patient and increases the risk of the development of drug-resistant bacteria.

Prolonged use of antibiotics may promote the overgrowth of nonsusceptible organisms, including fungi.
Should superinfection occur, appropriate measures should be taken.
Patients with gonorrhea who also have syphilis should be given additional appropriate parenteral penicillin treatment.
Treatment with ampicillin does not preclude the need for surgical procedures, particularly in staphylococcal infections.

Information for the patient

INFORMATION FOR PATIENTS SECTION

  1. The patient should inform the physician of any history of sensitivity to allergens, including previous hypersensitivity reactions to penicillins and cephalosporins (see WARNINGS).
  2. The patient should discontinue ampicillin and contact the physician immediately if any side effect occurs (see WARNINGS).
  3. Ampicillin should be taken with a full glass (8 oz) of water, one-half hour before or two hours after meals.
  4. Diabetic patients should consult with the physician before changing diet or dosage of diabetes medication (see PRECAUTIONS, Drug/Laboratory Test Interactions).

Patients should be counseled that antibacterial drugs, including Ampicillin capsules and Ampicillin for Oral Suspension should only be used to treat bacterial infections. They do not treat viral infections (e.g. the common cold).

When Ampicilin capsules or Ampicillin for Oral Suspension are prescribed to treat a bacterial infection, patients should be told that, although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may:

(i) Decrease the effectiveness of the immediate treatment, and

(ii) Increase the likelihood that bacteria will develop resistance and will not be treatable by Ampicillin capsules and Ampicillin for Oral Suspension or other antibacterial drugs in the future

Laboratory Tests

LABORATORY TESTS SECTION

In prolonged therapy, and particularly with high dosage regimens, periodic evaluation of the renal, hepatic and hematopoietic systems is recommended. In streptococcal infections, therapy must be sufficient to eliminate the organism (10 days minimum); otherwise the sequelae of streptococcal disease may occur. Cultures should be taken following completion of treatment to determine whether streptococci have been eradicated. Cases of gonococcal infection with a suspected lesion of syphilis should have darkfield examinations ruling out syphilis before receiving ampicillin. Patients who do not have suspected lesions of syphilis and are treated with ampicillin should have a follow-up serologic test for syphilis each month for four months to detect syphilis that may have been masked from treatment for gonorrhea.

Drug Interactions

DRUG INTERACTIONS SECTION

When administered concurrently, the following drugs may interact with ampicillin:

Allopurinol - Increased possibility of skin rash; particularly in hyperuricemic patients may occur.

Bacteriostatic antibiotics - Chloramphenicol, erythromycins, sulfonamides, or tetracyclines may interfere with the bactericidal effect of penicillins. This has been demonstrated in vitro; however, the clinical significance of this interaction is not well-documented.

Oral contraceptives - May be less effective and increased breakthrough bleeding may occur.

Probenecid - May decrease renal tubular secretion of ampicillin resulting in increased blood levels and/or ampicillin toxicity.

Drug/Laboratory Test Interactions

DRUG & OR LABORATORY TEST INTERACTIONS SECTION

After treatment with ampicillin, a false-positive reaction for glucose in the urine may occur with copper sulfate tests (Benedict's solution, Fehling's solution, or Clinitest® tablets) but not with enzyme based tests such as Clinistix® and Tes-Tape® (Glucose Enzymatic Test Strip USP).

Carcinogenesis, Mutagenesis, Impairment of Fertility

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Long-term studies in animals have not been performed to evaluate carcinogenesis, mutagenesis, or impairment of fertility in males or females.

Pregnancy

PREGNANCY SECTION

Teratogenic Effects

Category B:

Reproduction studies in animals have revealed no evidence of impaired fertility or harm to the fetus due to penicillin. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, penicillin should be used during pregnancy only if clearly needed.

Labor and Delivery

LABOR & DELIVERY SECTION

Oral ampicillin-class antibiotics are poorly absorbed during labor. Studies in guinea pigs showed that intravenous administration of ampicillin slightly decreased the uterine tone and frequency of contractions, but moderately increased the height and duration of contractions. However, it is not known whether use of these drugs in humans during labor or delivery has immediate or delayed adverse effects on the fetus, prolongs the duration of labor, or increases the likelihood that forceps delivery or other obstetrical intervention or resuscitation of the newborn will be necessary.

Nursing Mothers

NURSING MOTHERS SECTION

Ampicillin-class antibiotics are excreted in milk. Ampicillin used by nursing mothers may lead to sensitization of infants; therefore, a decision should be made whether to discontinue nursing or to discontinue ampicillin, taking into account the importance of the drug to the mother.

Pediatric Use

PEDIATRIC USE SECTION

Penicillins are excreted primarily unchanged by the kidney; therefore, the incompletely developed renal function in neonates and young infants will delay the excretion of penicillin. Administration to neonates and young infants should be limited to the lowest dosage compatible with an effective therapeutic regime (see DOSAGE AND ADMINISTRATION).

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

As with other penicillins, it may be expected that untoward reactions will be essentially limited to sensitivity phenomena. They are more likely to occur in individuals who have previously demonstrated hypersensitivity to penicillin and in those with a history of allergy, asthma, hay fever or urticaria.

The following adverse reactions have been reported as associated with the use of ampicillin:

Gastrointestinal: glossitis, stomatitis, nausea, vomiting, enterocolitis, pseudomembranous colitis, and diarrhea. These reactions are usually associated with oral dosage forms of the drug.

Hypersensitivity Reactions: An erythematous, mildly pruritic, maculopapular skin rash has been reported fairly frequently. The rash, which usually does not develop within the first week of therapy, may cover the entire body including the soles, palms, and oral mucosa. The eruption usually disappears in three to seven days. Other hypersensitivity reactions that have been reported are: skin rash, pruritus, urticaria, erythema multiforme, and an occasional case of exfoliative dermatitis. Anaphylaxis is the most serious reaction experienced and has usually been associated with the parenteral dosage form of the drug.

NOTE: Urticaria, other skin rashes, and serum sickness-like reactions may be controlled by antihistamines, and, if necessary, systemic corticosteroids. Whenever such reactions occur, ampicillin should be discontinued unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to ampicillin therapy. Serious anaphylactoid reactions require emergency measures (see WARNINGS).

Liver: Moderate elevation in serum glutamic oxaloacetic transaminase (SGOT) has been noted, but the significance of this finding is unknown.

Hemic and Lymphatic Systems: anemia, thrombocytopenia, thrombocytopenic purpura, eosinophilia, leukopenia, and agranulacytosis have been reported during therapy with penicillins. These reactions are usually reversible on discontinuation of therapy and are believed to be hypersensitivity phenomena.

Other adverse reactions that have been reported with the use of ampicillin are laryngeal stridor and high fever. An occasional patient may complain of sore mouth or tongue as with any oral penicillin preparation.

OVERDOSAGE

OVERDOSAGE SECTION

In case of overdosage, discontinue medication, treat symptomatically and institute supportive measures as required. In patients with renal function impairment, ampicillin-class antibiotics can be removed by hemodialysis but not by peritoneal dialysis.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Adults and children weighing over 20 Kg: For genitourinary or gastrointestinal tract infections other than gonorrhea in men and women, the usual dose is 500 mg q.i.d. in equally spaced doses; severe or chronic infections may require larger doses. For the treatment of gonorrhea in both men and women, a single oral dose of 3.5 grams of ampicillin administered simultaneously with 1 gram of probenecid is recommended. Physicians are cautioned to use no less than the above recommended dosage for the treatment of gonorrhea. Follow-up cultures should be obtained from the original site(s) of infection 7 to 14 days after therapy. In women, it is also desirable to obtain culture test-of-cure from both the endocervical and anal canals. Prolonged intensive therapy is needed for complications such as prostatitis and epididymitis. For respiratory tract infections, the usual dose is 250 mg q.i.d. in equally spaced doses.

Pediatric Patients weighing 20 Kg or less: For genitourinary or gastrointestinal tract infections, the usual dose is 100 mg/kg/day total, q.i.d. in equally divided and spaced doses.

For respiratory tract infections, the usual dose is 50 mg/kg/day total, in equally divided and spaced doses three to four times daily. Doses for children should not exceed doses recommended for adults.

All patients, irrespective of age and weight: Larger doses may be required for severe or chronic infections. Although ampicillin is resistant to degradation by gastric acid, it should be administered at least one half-hour before or two hours after meals for maximal absorption. Except for the single dose regimen for gonorrhea referred to above, therapy should be continued for a minimum of 48 to 72 hours after the patient becomes asymptomatic or evidence at bacterial eradication has been obtained. In infections caused by haemolytic strains of streptococci, a minimum of 10 days' treatment is recommended to guard against the risk of rheumatic fever or glomerulonephritis (see PRECAUTIONS, Laboratory Tests). In the treatment of chronic urinary or gastrointestinal infections, frequent bacteriologic and clinical appraisal is necessary during therapy and may be necessary for several months afterwards. Stubborn infections may require treatment for several weeks. Smaller doses than those indicated above should not be used.

HOW SUPPLIED

HOW SUPPLIED SECTION

Ampicillin Capsules, USP 500 mg: Each capsule contains ampicillin trihydrate equivalent to 500 mg ampicillin. The number 0 size capsule has a gray opaque body with a light blue opaque cap, printed WC404.

Bottles of 100 NDC 67253-181-10
Bottles of 500 NDC 67253-181-50

Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

Manufactured for: DAVA Pharmaceuticals, Inc .
Fort Lee, NJ 07024, USA

by: STADA Production Ireland Ltd.
Clonmel, Ireland.

Rev. 01/11

181G451

PACKAGE/LABEL PRINCIPLE DISPLAY PANEL – 500 mg - 500 capsules

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display Panel front - Ampicillin Capsules, USP 500 mg 500 capsules bottle
Principle Display Panel front - Ampicillin Capsules, USP 500 mg 500 capsules bottle

NDC 67253-181-50

AMPICILLIN

CAPSULES, USP

500 mg

500 capsules Rx only

Each capsule contains ampicillin trihydrate equivalent to 500 mg ampicillin.

Usual Adult Dosage -

250 mg - 500 mg 4 times a day in equally spaced doses. See package insert.

PHARMACY STOCK PACKAGE

Dispense in a tight, light-resistant container as defined in the USP.

Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

181J451

Manufactured for:

DAVA Pharmaceuticals, Inc.

Fort Lee, NJ 07024 USA

by:

STADA Production Ireland Ltd.

Clonmel, Ireland

181G451

Rev. 01/11

Repacked by:

H.J. Harkins Company, Inc.

Grover Beach, CA 93433

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308212ampicillin 500 MG Oral CapsulePSN1
308212ampicillin 500 MG Oral CapsuleSCD1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
AMPICILLIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fd9d6ee0-43ae-43c7-aa52-3d5a936186d6Product name120250722
4fe9b92f-7dcd-4058-8def-e75f4dcd5ab3Product name220160201
c9385d77-2af7-47a4-bc97-1127e71caf9bProduct name320160201
05b6b9ae-4ba4-27ee-4c8c-f72b41de3815Product name520151207
b353113e-7b3d-4b1f-a286-b96a3a5eac85Product name320151026
8c59be9b-72b0-49e8-b7ef-1a80c10599deProduct name320150316

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52959-389-20Ampicillin20 in 1 BOTTLE, PLASTICCAPSULE201
52959-389-28Ampicillin28 in 1 BOTTLE, PLASTICCAPSULE281
52959-389-30Ampicillin30 in 1 BOTTLE, PLASTICCAPSULE301
52959-389-40Ampicillin40 in 1 BOTTLE, PLASTICCAPSULE401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52959-389AMPICILLIN CAPSULE [H.J. HARKINS COMPANY, INC.]1Legacy NDC, 4 package rows20120829_e6040d92-0b8f-4808-a375-eece4aeeff18.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52959-389-20EA - Each52959-389c7e99b41-aedf-497d-8012-386617cd719612013-02-13
52959-389-28EA - Each52959-389a7178d43-207f-445e-b860-34b1e950706e12013-02-13
52959-389-30EA - Each52959-389ecb6b451-8655-4ced-9a07-97d4d78acc3a12013-02-13
52959-389-40EA - Each52959-389b49817ce-e7d8-4d27-b8a9-4f01583bad1b12013-02-13
67253-181-10EA - Each67253-181b6d6d589-6625-4d67-9cc4-a945c418080612012-07-24
67253-181-50EA - Each67253-18125e8382f-947d-4c29-9903-3a02fa4b7ad412012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMPICILLIN TRIHYDRATEACTIVE INGREDIENTHXQ6A1N7R61
AMPICILLINACTIVE MOIETY7C782967RD1
D&C RED NO. 28INACTIVE INGREDIENT767IP0Y5NH1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBD1
FERROSOFERRIC OXIDEINACTIVE INGREDIENTXM0M87F3571
GELATININACTIVE INGREDIENT2G86QN327L1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU41
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141J1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JP1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52959-38952959-389-20, 52959-389-28, 52959-389-30, 52959-389-40
67253-181

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 5 · 272 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, COATED / ORAL49 mgExact identifier — unii candidate
40 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL3 mgExact identifier — unii candidate
42 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPSUPPOSITORY, EXTENDED RELEASE / INTRAUTERINE1 mgExact identifier — unii candidate
40 equally ranked IID candidates
GELATINGELATIN2G86QN327LINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS14 mgExact identifier — unii candidate
44 equally ranked IID candidates
D&C RED NO. 28D&C RED NO. 28767IP0Y5NHCAPSULE / ORAL1 mgExact identifier — unii candidate
11 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPCREAM / TOPICAL80 mgExact identifier — unii candidate
40 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDTABLET / SUBLINGUAL0.03 mgExact identifier — unii candidate
37 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET, EXTENDED RELEASE / ORAL173 mgExact identifier — unii candidate
39 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4SUPPOSITORY / RECTAL14 mgExact identifier — unii candidate
49 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JLOTION / TOPICAL111 mgExact identifier — unii candidate
42 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30SYSTEM / INTRAVITREAL0.02 mgExact identifier — unii candidate
39 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30POWDER / TOPICAL104 mgExact identifier — unii candidate
39 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET, CHEWABLE, EXTENDED RELEASE / ORAL2 mgExact identifier — unii candidate
49 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET, CHEWABLE, EXTENDED RELEASE / ORAL9 mgExact identifier — unii candidate
39 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4GRANULE, DELAYED RELEASE / ORAL3.2 mgExact identifier — unii candidate
49 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPCAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
40 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDLIQUID / ORALNAExact identifier — unii candidate
37 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPCAPSULE / ORAL72 mgExact identifier — unii candidate
40 equally ranked IID candidates
GELATINGELATIN2G86QN327LTABLET / ORAL46 mgExact identifier — unii candidate
44 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4CAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
49 equally ranked IID candidates
GELATINGELATIN2G86QN327LTABLET / SUBLINGUAL19 mgExact identifier — unii candidate
44 equally ranked IID candidates
GELATINGELATIN2G86QN327LSOLUTION / ORAL34.8 mgExact identifier — unii candidate
44 equally ranked IID candidates
D&C RED NO. 28D&C RED NO. 28767IP0Y5NHPOWDER, FOR SUSPENSION / ORAL0.7 mg/5mlExact identifier — unii candidate
11 equally ranked IID candidates
GELATINGELATIN2G86QN327LINJECTION / INTRAVENOUS20 mgExact identifier — unii candidate
44 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDSOLUTION / DENTALNAExact identifier — unii candidate
37 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, CHEWABLE / ORAL6 mgExact identifier — unii candidate
42 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDLIQUID / TOPICALNAExact identifier — unii candidate
37 equally ranked IID candidates
D&C RED NO. 28D&C RED NO. 28767IP0Y5NHCAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
11 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JPOWDER / RESPIRATORY (INHALATION)NAExact identifier — unii candidate
42 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30PELLET / ORAL24 mgExact identifier — unii candidate
39 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET / SUBLINGUAL10 mgExact identifier — unii candidate
49 equally ranked IID candidates
GELATINGELATIN2G86QN327LTABLET, CHEWABLE / ORAL24 mgExact identifier — unii candidate
44 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDELIXIR / ORALNAExact identifier — unii candidate
37 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCAPSULE / ORAL600 mgExact identifier — unii candidate
42 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30LOZENGE / TRANSMUCOSAL100 mgExact identifier — unii candidate
39 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4POWDER, FOR SUSPENSION / ORAL2553 mgExact identifier — unii candidate
49 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDFILM, SOLUBLE / ORAL0.04 mgExact identifier — unii candidate
37 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4SYSTEM / TRANSDERMAL35 mgExact identifier — unii candidate
49 equally ranked IID candidates
GELATINGELATIN2G86QN327LDROPS / NASAL50 mg/1mlExact identifier — unii candidate
44 equally ranked IID candidates
GELATINGELATIN2G86QN327LINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR14 mgExact identifier — unii candidate
44 equally ranked IID candidates
GELATINGELATIN2G86QN327LCAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
44 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDPASTE / DENTALNAExact identifier — unii candidate
37 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JGRANULE / ORAL12 mgExact identifier — unii candidate
42 equally ranked IID candidates
GELATINGELATIN2G86QN327LINJECTION, SUSPENSION / INTRAMUSCULAR1.3 mgExact identifier — unii candidate
44 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL42 mgExact identifier — unii candidate
40 equally ranked IID candidates
GELATINGELATIN2G86QN327LGUM, CHEWING / BUCCAL102 mgExact identifier — unii candidate
44 equally ranked IID candidates
GELATINGELATIN2G86QN327LWAFER / ORALNAExact identifier — unii candidate
44 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPCAPSULE, LIQUID FILLED / ORAL12 mgExact identifier — unii candidate
40 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDPASTE, DENTIFRICE / DENTALNAExact identifier — unii candidate
37 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JDROPS / ORALNAExact identifier — unii candidate
42 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, DELAYED RELEASE / ORAL66 mgExact identifier — unii candidate
40 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, FILM COATED / ORAL240 mgExact identifier — unii candidate
42 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JPELLET / ORAL2 mgExact identifier — unii candidate
42 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDSOLUTION / TOPICAL0.01 %w/wExact identifier — unii candidate
37 equally ranked IID candidates
FERROSOFERRIC OXIDEFERROSOFERRIC OXIDEXM0M87F357CAPSULE, COATED / ORAL0.11 mgExact identifier — unii candidate
10 equally ranked IID candidates
FERROSOFERRIC OXIDEFERROSOFERRIC OXIDEXM0M87F357TABLET, FILM COATED / ORAL0.2 mgExact identifier — unii candidate
10 equally ranked IID candidates
FERROSOFERRIC OXIDEFERROSOFERRIC OXIDEXM0M87F357CAPSULE, DELAYED RELEASE / ORAL6 mgExact identifier — unii candidate
10 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JSHAMPOO, SUSPENSION / TOPICAL40 %w/vExact identifier — unii candidate
42 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30CAPSULE, DELAYED RELEASE / ORAL1060 mgExact identifier — unii candidate
39 equally ranked IID candidates
GELATINGELATIN2G86QN327LCAPSULE, COATED PELLETS / ORAL65 mgExact identifier — unii candidate
44 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A062882-001AMPICILLIN TRIHYDRATEAMPICILLIN/AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25

Observed Orange Book product history#

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.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-2584e616aacf4f…
2026-08-18 06:07:402026-07A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-2531067a03dcf5…
2025-08-23 18:47 UTC2025-08A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-256a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-2503ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-252680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-255bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-2579d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-251e350fbaab3a…
2024-05-31 18:47 UTC2024-05A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-258072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-255c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-255d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-254b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORALABRS1988-02-2574a2ff9319b5…
2022-03-09 01:35 UTC2022-03A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-2587673890dc5c…
2021-03-12 10:30 UTC2021-03A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-255aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-258869cabd3fbd…
2020-11-12 02:37 UTC2020-11A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25c0c555d07b60…
2019-12-14 00:12 UTC2019-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORALABRS1988-02-253f01610625f2…
2019-09-15 20:21 UTC2019-09A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORALABRS1988-02-25b00525d2431f…
2019-07-19 19:46 UTC2019-07A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORALABRS1988-02-25ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-256a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-251c564ffb4f44…
2023-12-20 04:57 UTC2023-12A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-259b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-253f0d92c62455…
2023-05-13 08:27 UTC2023-05A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25053a50430f4f…
2023-01-26 05:58 UTC2023-01A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-253bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-253a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A062882-001AMPICILLIN TRIHYDRATEEQ 500MG BASECAPSULE / ORAL1988-02-25f41ea6bd6efb…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2019-12-13 00:20 UTC2019-12A062882-001AB174a2ff9319b5…
2019-12-14 00:12 UTC2019-12A062882-001AB13f01610625f2…
2019-09-15 20:21 UTC2019-09A062882-001AB1b00525d2431f…
2019-07-19 19:46 UTC2019-07A062882-001AB1ea99ee380514…

openFDA label cross-check#

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
8cd46ed0-6629-479f-9c35-22fbeb811d71e6040d92-0b8f-4808-a375-eece4aeeff182012-08-28Warnings, Adverse reactionsExact identifier
spl id: 8cd46ed0-6629-479f-9c35-22fbeb811d71
spl set id: e6040d92-0b8f-4808-a375-eece4aeeff18

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.