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TRIPLE ANTIBIOTIC - 59450-034-32 - (bacitracin zinc neomycin sulfate polymyxin b sulfate)

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Drug Information of TRIPLE ANTIBIOTIC

Product NDC: 59450-034
Proprietary Name: TRIPLE ANTIBIOTIC
Non Proprietary Name: bacitracin zinc neomycin sulfate polymyxin b sulfate
Active Ingredient(s): 400; 3.5; 5000    [iU]/g; mg/g; [iU]/g & nbsp;   bacitracin zinc neomycin sulfate polymyxin b sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of TRIPLE ANTIBIOTIC

Product NDC: 59450-034
Labeler Name: The Kroger Co.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030101

Package Information of TRIPLE ANTIBIOTIC

Package NDC: 59450-034-32
Package Description: 1 TUBE in 1 CARTON (59450-034-32) > 56 g in 1 TUBE

NDC Information of TRIPLE ANTIBIOTIC

NDC Code 59450-034-32
Proprietary Name TRIPLE ANTIBIOTIC
Package Description 1 TUBE in 1 CARTON (59450-034-32) > 56 g in 1 TUBE
Product NDC 59450-034
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacitracin zinc neomycin sulfate polymyxin b sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20030101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Kroger Co.
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit [iU]/g; mg/g; [iU]/g
Pharmaceutical Classes

Complete Information of TRIPLE ANTIBIOTIC


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