VACASAN 25- tulathromycin injection, solution
VACASAN 25 by
Drug Labeling and Warnings
VACASAN 25 by is a Animal medication manufactured, distributed, or labeled by Huvepharma, Inc., Parnell Manufacturing Pty Ltd. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
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DESCRIPTION
DESCRIPTION
VACASAN™ 25 Injectable Solution is a ready-to-use sterile parenteral preparation containing tulathromycin, a semi-synthetic macrolide antibiotic of the subclass triamilide. Each mL of VACASAN™ 25 contains 25 mg of tulathromycin as the free base in 50% propylene glycol vehicle, monothioglycerol (5 mg/mL), citric acid (4.8 mg/mL) with hydrochloric acid and sodium hydroxide added to adjust pH. VACASAN™ 25 consists of an equilibrated mixture of two isomeric forms of tulathromycin in a 9:1 ratio.
The chemical names of the isomers are (2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-13-[[2,6-dideoxy-3-C-methyl-3-O-methyl-4-C-[(propylamino) methyl]-α-L-ribo-hexopyrano-syl]oxy]-2-ethyl-3,4,10-trihydroxy-3,5,8,10,12,14-hexamethyl-11-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]-oxy]-1-oxa-6-azacyclopentadecan-15-one and (2R,3R,6R,8R,9R,10S,11S,12R)-11-[[2,6-dideoxy-3-C-methyl- 3-O-methyl-4-C-[(propylamino)methyl]- α-L-ribo-hexopyrano-syl]oxy]-2-[(1R,2R)-1,2-dihydroxy-1-methylbutyl]-8-hydroxy-3,6,8,10,12-pentamethyl-9-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-1-oxa-4-azacyclotridecan-13-one, respectively.
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INDICATIONS & USAGE
INDICATIONS
Swine
VACASAN™ 25 Injectable Solution is indicated for the treatment of swine respiratory disease (SRD)
associated with Actinobacillus pleuropneumoniae, Pasteurella multocida, Bordetella bronchiseptica,
Haemophilus parasuis, and Mycoplasma hyopneumoniae; and for the control of SRD associated with
Actinobacillus pleuropneumoniae, Pasteurella multocida, and Mycoplasma hyopneumoniae in groups of
pigs where SRD has been diagnosed.Suckling Calves, Dairy Calves, and Veal Calves
BRD – VACASAN 25 Injectable Solution is indicated for the treatment of bovine respiratory disease (BRD) associated with
Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, and Mycoplasma bovis. -
DOSAGE & ADMINISTRATION
DOSAGE AND ADMINISTRATION
Swine
Inject intramuscularly as a single dose in the neck at a dosage of 2.5 mg/kg (1 mL/22 lb) body weight (BW).
Do not inject more than 4 mL per injection site.Table 1. VACASAN 25 Swine Dosing Guide (25mg/mL)
Animal Weight (Pounds) Dose Volume (mL) 4 0.2 10 0.5 15 0.7 20 0.9 22 1.0 25 1.1 30 1.4 50 2.3 70 3.2 90 4.0 - DOSAGE & ADMINISTRATION
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WARNINGS AND PRECAUTIONS
WARNINGS
FOR USE IN ANIMALS ONLY.
NOT FOR HUMAN USE.
KEEP OUT OF REACH OF CHILDREN.
NOT FOR USE IN CHICKENS OR TURKEYS.RESIDUE WARNINGS
Swine
Swine intended for human consumption must not be slaughtered within 5 days from the last treatment.
Calves
Calves intended for human consumption must not be slaughtered within 22 days from the last treatment with VACASAN 25 Injectable Solution. This drug is not for use in ruminating cattle.
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WARNINGS AND PRECAUTIONS
PRECAUTIONS
Swine
The effects of VACASAN™ 25 Injectable Solution on porcine reproductive performance, pregnancy, and lactation have not been determined. Intramuscular injection can cause a transient local tissue reaction that may result in trim loss of edible tissue at slaughter.
Cattle
The effects of VACASAN™ 25 Injectable Solution on bovine reproductive performance, pregnancy, and lactation have not been determined. Subcutaneous injection can cause a transient local tissue reaction that may result in trim loss of edible tissue at slaughter.
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ADVERSE REACTIONS
ADVERSE REACTIONS
Swine
In one field study, one out of 40 pigs treated with tulathromycin injection (100 mg/mL)at 2.5 mg/kg BW exhibited mild salivation that resolved in less than four hours.
Calves
In one BRD field study, two calves treated with tulathromycin injection (100 mg/mL) at 2.5 mg/kg BW exhibited transient hypersalivation. One of these calves also exhibited transient dyspnea, which may have been related to pneumonia.
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90375-7 - Section Title Not Found In Database
POST APPROVAL EXPERIENCE
The following adverse events are based on post approval adverse drug experience reporting for tulathromycin injection (100 mg/mL). Not all adverse events are reported to the FDA CVM. It is not always possible to reliably estimate the adverse event frequency or establish a causal relationship to product exposure using these data. The following adverse events are listed in decreasing order of reporting frequency in cattle: Injection site reactions and anaphylaxis/anaphylactoid reactions. For a complete listing of adverse reactions for tulathromycin injection 100 mg/mL or tulathromycin injection 25 mg/mL reported to the CVM see: www.fda.gov/reportanimalae.
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CLINICAL PHARMACOLOGY
CLINICAL PHARMACOLOGY
At physical pH, tulathromycin (a weak base) is approximately 50 times more soluble in hydrophilic than hydrophobic media. This solubility profile is consistent with the extracellular pathogen activity typically associated with the macrolides.1 Markedly higher tulathromycin concentrations are observed in the lungs as compared to plasma. The extent to which lung concentrations represent free (active) drug was not examined. Therefore, the clinical relevance of these elevated lung concentrations is undetermined.
As a class, macrolides tend to be primarily bacteriostatic, but may be bactericidal against some pathogens.2 When acting as a cidal compound, they tend to exhibit concentration independent killing; the rate of bacterial eradication does not change once serum drug concentrations reach 2 to 3 times the minimum inhibitory concentration (MIC) of the targeted pathogen. Under these conditions, the tiime that serum concentrations remain above the MIC becomes the major determinant of antimicrobial activity. Macrolides also exhibit a post-antibiotic effect (PAE), the duration of which tends to be both drug and pathogen dependent. In general, by increasing the macrolide concentration and the exposure time, the PAE will increase to some maximal duration.3 Tulathromycin is eliminated from the body primarily unchanged via biliary excretion.
1Carbon, C. 1998. Pharmacodynamics of Macrolides, Azalides, and Streptogramins: Effect on Extracellular Pathogens. Clin. Infect. Dis., 27:28-32.
2Nightingale, C.J. 1997. Pharacokinetics and Pharmacodynamics of Newer Macrolides. Pediatr. Infect. Dis. J., 16:438-443.
3Andes D, Anon J, Jacobs MR, Craig, WA. (2004). Application of pharmacokinetics and pharmacodynamics to antimicrobial therapy of respiratory tract infections. Clin Lab Med., 24:477-502.
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CLINICAL PHARMACOLOGY
Swine
Following intramuscular (IM) administration to feeder pigs at a dosage of 2.5 mg/kg BW, tulathromycin is nearly completely absorbed, with peak plasma concentrations achieved within ~0.25 hr. The volume of distribution exceeds 15 L/kg, which is consistent with extensive tissue binding. This large distribution volume results in a long terminal elimination half-life (60 to 90 hours) despite a rapid systemic free drug clearance (187 mL/kg/hr). There are no gender differences in swine tulathromycin pharmacokinetics.
Comparative Bioavailability Summary
Despite slightly lower peak concentrations with tulathromycin injection 25 mg/mL, a single IM dose of 2.5 mg tulathromycin/kg BW of either tulathromycin injection (100 mg/mL) or tulathromycin injection (25 mg/mL) resulted in comparable tulathromycin total systemic exposure. Therefore, tulathromycin injection 25 mg/mL is considered to be therapeutically equivalent to tulathromycin injection 100 mg/mL when administered to swine by IM injection at a dose of 2.5 mg tulathromycin/kg BW.
Calves
Following subcutaneous (SC) administration into the neck of feeder calves at a dosage of 2.5 mg/kg BW, tulathromycin is nearly completely absorbed, with peak plasma concentrations achieved within ~0.25 hr. The volume of distribution exceeds 11 L/kg4, which is consistent with extensive tissue binding. This large distribution volume results in a long terminal elimination half-life of more than 100 hours, despite a rapid systemic free drug clearance (170 mL/kg/hr). No pharmacokinetic differences are observed in castrated male versus female calves.
Comparative Bioavailability Summary
Despite lower peak concentrations with tulathromycin 25 mg/mL, a single SC dose of 2.5 mg tulathromycin/kg BW of either tulathromycin injection (100 mg/mL) or tulathromycin injection (25 mg/mL) resulted in comparable total systemic tulathromycin exposure. Therefore, tulathromycin injection 25 mg/mL is considered to be therapeutically equivalent to tulathromycin injection 100 mg/mL when administered to calves by SC injection at a dose of 2.5 mg tulathromycin/kg BW.
4Clearance and volume estimates are based on inter subject comparisons of 2.5 mg/kg BW administered by either subcutaneous or intravenous injection.
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MICROBIOLOGY
MICROBIOLOGY
Swine
Tulathromycin has demonstrated in vitro activity against A. pleuropneumoniae, P. multocida, B. bronchiseptica, H. parasuis, and M. hyopneumoniae. The MICs of tulathromycin against indicated pathogens collected from field studies were determined using methods recommended by the Clinical and Laboratory Standards Institute (CLSI, M31-A and M31-A3). MICs for H. parasuis were determined using Veterinary Fastidious Medium and were incubated up to 48 hours at 35 to 37°C in a CO2-enriched atmosphere. These values are represented in Table 3, below.
Table 3. Tulathromycin minimum inhibitory concentration (MIC) values* for indicated pathogens isolated from field studies evaluating SRD in the U.S. and Canada.
Indicated pathogen Date Isolated No. of isolates MIC50** (μg/mL) MIC90** (μg/mL) MIC range (μg/mL) Actinobacillus pleuropneumoniae 2000-2002
2007-2008135
88
16
16
32
16
16 to 32 4 to 32
Haemophilus parasuis 2000-2002 31 1 2 0.25 to >64 Pasteurella multocida 2000-2002
2007-200855
40
1
1
2
2
0.5 to >64 ≤ 0.03 to 2
Bordetella bronchiseptica 2000-2002 42 4 8 2 to 8 * The correlation between in vitro susceptibility data and clinical effectiveness is unknown.** The lowest MIC to encompass 50% and 90% of the most susceptible isolates, respectively.
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MICROBIOLOGY
Calves
Tulathromycin has demonstrated in vitro activity against M. haemolytica, P. multocida, H. somni, and M. bovis, four pathogens associated with BRD. The MICs of tulathromycin against indicated pathogens collected from field studies using tulathromycin injection (100 mg/mL) were determined using methods recommended by the CLSI (M31-A2). These values are represented in Table 4, below.
Table 4. Tulathromycin minimum inhibitory concentration (MIC) values* for indicated pathogens isolated from field studies evaluating BRD in the U.S.
Indicated pathogen Date Isolated No. of isolates MIC50** (μg/mL) MIC90** (μg/mL) MIC range (μg/mL) Mannheimia haemolytica 1999 642 2 2 0.5 to 64 Pasteurella multocida 1999 221 0.5 1 0.25 to 64 Histophilus somni 1999 36 4 4 1 to 4 Mycoplasma bovis 1999 43 0.125 1 ≤ 0.063 to > 64 * The correlation between in vitro susceptibility data and clinical effectiveness is unknown.** The lowest MIC to encompass 50% and 90% of the most susceptible isolates, respectively.
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SUMMARY OF SAFETY AND EFFECTIVENESS
EFFECTIVENESS
Swine
Plasma concentrations of tulathromycin administered as tulathromycin injection (100 mg/mL) or as tulathromycin injection 25 mg/mL were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore, effectiveness studies conducted with tulathromycin injection (100 mg/mL) support the effectiveness for tulathromycin injection 25 mg/mL. In a multi-location field study to evaluate the treatment of naturally occuring SRD, 266 pigs were treated with tulathromycin injection (100 mg/mL). Responses to treatment were compared to saline-treated controls. Success was defined as a pig with normal attitude, normal respiration, and rectal temperature of < 104°F on Day 7. The treatment success rate was significantly greater (P ≤ 0.05) in tulathromycin injection 100 mg/mL-treated pigs (70.5%) compared to saline-treated pigs (46.1%). M. hyopneumoniae was isolated from 106 saline-treated and non-treated sentinel pigs in this study.
Two induced infection model studies were conducted to confirm the effectiveness of tulathromycin injection (100 mg/mL) against M. hyopneumoniae. Ten days after inoculation intranasally and intratracheally with a field strain of M. hyopneumoniae, 144 pigs were treated with either tulathromycin injection 100 mg/mL (2.5 mg/kg BW) intramuscularly or an equivalent volume of saline. Pigs were euthanized and necropsied 10 days post-treatment. The mean percentage of gross pneumonic lung lesions was statistically significantly lower (P < 0.0001) for tulathromycin injection 100 mg/mL-treated pigs than for saline-treated pigs in both studies (8.52% vs. 23.62% and 11.31% vs. 26.42%).
The effectiveness of tulathromycin injection (100 mg/mL) for the control of SRD was evaluated in a multi-location natural infection field study. When at least 15% of the study candidates showed clinical signs of SRD, all pigs were enrolled and treated with tulathromycin injection 100 mg/mL (226 pigs) or saline (227 pigs). Responses to treatment were evaluated on Day 7. Success was defined as a pig with normal attitude, normal respiration, and rectal temperature of < 104°F. The treatment success rate was significantly greater (P < 0.05) in tulathromycin injection 100 mg/mL-treated pigs compared to saline-treated pigs (59.2% vs. 41.2%).
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SUMMARY OF SAFETY AND EFFECTIVENESS
Calves
Plasma concentrations of tulathromycin administered as tulathromycin injection (100 mg/mL) or as tulathromycin injection 25 mg/mL were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore, effectiveness studies conducted with tulathromycin injection (100 mg/mL) support the effectiveness for tulathromycin injection 25 mg/mL.
BRD- In a multi-location field study, 314 calves with naturally occurring BRD were treated with tulathromycin injection. Responses to treatment were compared to saline-treated controls. A cure was defined as a calf with normal attitude/activity, normal respiration, and a rectal temperature of ≤ 104°F on Day 14. The cure rate was significantly higher (P ≤ 0.05) in tulathromycin injection 100 mg/mL-treated calves (78%) compared to saline-treated calves (24%). There were two BRD-related deaths in the tulathromycin injection 100 mg/mL-treated calves compared to nine BRD-related deaths in the saline-treated calves.
Fifty-two tulathromycin injection (100 mg/mL)-treated calves and 27 saline-treated calves from the multi-location field BRD treatment study had Mycoplasma bovis identified in cultures from pre-treatment nasopharyngeal swabs. Of the 52 tulathromycin injection 100 mg/mL-treated calves, 37 (71.2%) calves were categorized as cures and 15 (28.8%) calves were categorized as treatment failures. Of the 27 saline-treated calves, 4 (14.8%) calves were categorized as cures and 23 (85.2%) calves were treatment failures.
A Bayesian meta-analysis was conducted to compare the BRD treatment success rate in young calves (calves weighing 250 lbs or less and fed primarily a milk-based diet) treated with tulathromycin injection (100 mg/mL) to the success rate in older calves (calves weighing more than 250 lbs and fed primarily a roughage and grain-based diet) treated with tulathromycin injection 100 mg/mL. The analysis included data from four BRD treatment effectiveness studies conducted for the approval of tulathromycin injection (100 mg/mL) in the U.S. and nine contemporaneous studies conducted in Europe. The analysis showed that the BRD treatment success rate in young calves was at least as good as the BRD treatment success rate in older calves. As a result, tulathromycin injection (100 mg/mL) was considered effective for the treatment of BRD associated with M. haemolytica, P.multocida, H. somni, and M. bovis in suckling calves, dairy calves, and veal calves.
Two induced infection model studies were conducted to confirm the effectiveness of tulathromycin injection (100 mg/mL) against Mycoplasma bovis. A total of 166 calves were inoculated intratracheally with field strains of Mycoplasma bovis. When calves became pyrexic and had abnormal respiration scores, they were treated with either tulathromycin injection (100 mg/mL) (2.5 mg/kg BW) subcutaneously or an equivalent volume of saline. Calves were observed for signs of BRD for 14 days post-treatment, then were euthanized and necropsied. In both studies, mean lung lesion percentages were statistically significantly lower in the tulathromycin injection 100 mg/mL-treated calves compared with saline-treated calves (11.3% vs. 28.9%, P = 0.0001 and 15.0% vs. 30.7%, P < 0.0001).
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SUMMARY OF SAFETY AND EFFECTIVENESS
ANIMAL SAFETY
Swine
Plasma concentrations of tulathromycin administered as tulathromycin injection (100 mg/mL) or as tulathromycin injection 25 mg/mL were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore, systemic target animal safety studies conducted with tulathromycin injection 100 mg/mL support the systemic safety for tulathromycin injection 25 mg/mL.
Safety studies were conducted in pigs receiving a single intramuscular dose of 25 mg/kg BW, or 3 weekly intramuscular doses of 2.5, 7.5, or 12.5 mg/kg BW (both studies utilized tulathromycin injection (100 mg/mL)). In all groups, transient indications of pain after injection were seen, including restlessness and excessive vocalization. Tremors occurred briefly in one animal receiving 7.5 mg/ kg BW. Discoloration and edema of injection site tissues and corresponding histopathologic changes were seen in animals at all dosages and resolved over time. No other drug-related lesions were observed macroscopically or microscopically.
Sixteen growing pigs were injected with either saline or tulathromycin injection 25 mg/mL as a single injection of 4 mL. Injection site observations included two instances of erythema in the tulathromycin injection 25 mg/mL-treated group on Day 1 post-injection. No heat, sensitivity, firmness, necrosis, drainage, or swelling was observed at any injection sites in either treatment group. The gross and microscopic findings in the tulathromycin injection 25 mg/mL-treated group were consistent with inflammatory changes induced by injections and were considered to be mild or moderate with progression to macroscopic resolution by Day 28 post-injection and microscopic resolution by Day 42 post-injection.
Calves
Plasma concentrations of tulathromycin administered as tulathromycin administered as tulathromycin injection (100 mg/mL) or as tulathromycin injection 25 mg/mL were demonstrated to be therapeutically equivalent (see CLINICAL PHARMACOLOGY, Comparative Bioavailability Summary). Therefore, systemic target animal safety studies conducted with tulathromycin injection 100 mg/mL support the systemic safety for tulathromycin injection 25 mg/mL.
A safety study was conducted in feeder calves receiving tulathromycin injection (100 mg/mL) as a single subcutaneous dose of 25 mg/kg BW, or 3 weekly subcutaneous doses of 2.5, 7.5, or 12.5 mg/kg BW. In all groups, transient indications of pain after injection were seen, including head shaking and pawing at the ground. Injection site swelling, discoloration of the subcutaneous tissues at the injection site and corresponding histopathologic changes were seen in animals in all dosage groups. These lesions showed signs of resolving over time. No other drug-related lesions were observed macroscopically or microscopically.
An exploratory study was conducted in feeder calves receiving tulathromycin injection (100 mg/mL) as a single subcutaneous dose of 10, 12.5, or 15 mg/kg BW. Macroscopically, no lesions were observed. Microscopically, minimal to mild myocardial degeneration was seen in one of six calves administered 12.5 mg/kg BW and two of six calves administered 15 mg/kg BW.
A safety study was conducted in preruminant calves 13 to 27 days of age receiving tulathromycin injection (100 mg/mL) at 2.5 mg/kg BW or 7.5 mg/kg BW once subcutaneously. With the exception of minimal to mild injection site reactions, no drug-related clinical signs or other lesions were observed macroscopically or microscopically.
Sixteen growing cattle were injected with either saline (eight animals) as a single injection of 11.5 mL or tulathromycin injection 25 mg/mL (eight animals) as a single injection of either 2.5 mg/kg BW or a dose volume of 11.5 mL (whichever volume was higher). One calf in the tulathromycin injection 25 mg/mL-treated group was observed to have firmness at the injection site for a single day. Two tulathromycin injection 25 mg/mL- treated calves exhibited injection site swelling. In one calf, the swelling resolved within 48 hours. In the other calf, the swelling was observed over a three-day period, after which the calf underwent a scheduled necropsy, preventing further injection site observations. No injection site swelling was observed in saline-treated animals. At necropsy, three of the saline-treated calves and five of the tulathromycin injection 25 mg/mL-treated calves had altered tissue present at the injection site. The gross and microscopic findings in the tulathromycin injection 25 mg/mL-treated group were consistent with inflammatory changes induced by injections, were considered to be mild to marked, and progressed to macroscopic resolution and microscopic resolution by Day 42 post-injection.
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STORAGE AND HANDLING
STORAGE CONDITIONS
Store at or below 25°C (77°F).
100 mL - Use within 90 days of first vial puncture.
250 mL - Use within 90 days of the first puncture and puncture a maximum of 40 times. If more than 40 punctures are anticipated, the use of automatic injection equipment of a repeater syringe is recommended. When using a draw-off spike or needle with a bore diameter larger than 16-gauge, discard any product remaining in the vial immediately after use. -
HOW SUPPLIED
HOW SUPPLIED
VACASAN™ 25 Injectable Solution (tulathromycin injection) is available in the following package sizes:
100 mL vial
250 mL vialApproved by FDA under ANADA # 200-745
Manufactured for:
HUVEPHARMA, INC.
525 Westpark Drive, Suite 230
Peachtree City, GA 30269100mL: 50410b-01-10-2024250mL: 50411-01-10-2024
To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet, contact Huvepharma at 1-877-994-4883. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae.
For additional VACASAN™ 25 Product information contact Huvepharma at 1-877-994-4883 or go to www.huvepharma.us.
VACASAN™ is a trademark of Huvepharma, Inc.
50410b-01 50411-01
Rev. 10-2024 Rev. 10-2024 -
PRINCIPLE DISPLAY PANEL - 100 mL Bottle
VACASAN™ 25
(tulathromycin injection)
Injectable Solution
Antibiotic
25 mg of tulathromycin/mL
For use in suckling calves, dairy calves, veal calves, and swine.
Not for use in ruminating cattle.CAUTION: Federal (U.S.A.) law restricts this drug to use
by or on the order of a licensed veterinarian.Net Contents: 100 mL
Approved by FDA under ANADA # 200-745
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PRINCIPLE DISPLAY PANEL - 100 mL Carton
VACASAN™ 25
(tulathromycin injection)
Injectable Solution
Antibiotic
25 mg of tulathromycin/mL
For use in suckling calves, dairy calves, veal calves, and swine.
Not for use in ruminating cattle.
CAUTION: Federal (U.S.A.) law restricts this drug to use
by or on the order of a licensed veterinarian.Net Contents: 100 mL
Approved by FDA under ANADA # 200-745
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PRINCIPLE DISPLAY PANEL - 250 mL Bottle
VACASAN™ 25
(tulathromycin injection)
Injectable Solution
Antibiotic
25 mg of tulathromycin/mL
For use in suckling calves, dairy calves, veal calves, and swine.
Not for use in ruminating cattle.CAUTION: Federal (U.S.A.) law restricts this drug to use
by or on the order of a licensed veterinarian.Net Contents: 250 mL
Approved by FDA under ANADA # 200-745
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INGREDIENTS AND APPEARANCE
VACASAN 25
tulathromycin injection, solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC: 23243-2825 Route of Administration INTRAMUSCULAR, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TULATHROMYCIN (UNII: Q839I13422) (TULATHROMYCIN - UNII:Q839I13422) TULATHROMYCIN 25 mg in 1 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 500 mg in 1 mL MONOTHIOGLYCEROL (UNII: AAO1P0WSXJ) 5 mg in 1 mL ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 19.2 mg in 1 mL HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 23243-2825-1 1 in 1 CARTON 1 100 mL in 1 VIAL, MULTI-DOSE 2 NDC: 23243-2825-2 250 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200745 04/03/2023 Labeler - Huvepharma, Inc. (619153559) Establishment Name Address ID/FEI Business Operations Parnell Manufacturing Pty Ltd 742511488 manufacture, analysis, sterilize, label
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