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Triple Antibiotic - 0603-0644-50 - (bacitracin zinc and neomycin sulfate and polymyxin b sulfate)

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Drug Information of Triple Antibiotic

Product NDC: 0603-0644
Proprietary Name: Triple Antibiotic
Non Proprietary Name: bacitracin zinc and neomycin sulfate and polymyxin b sulfate
Active Ingredient(s): 400; 3.5; 5000    [USP'U]/g; mg/g; [USP'U]/g & nbsp;   bacitracin zinc and neomycin sulfate and polymyxin b sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 0603-0644
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19970801

Package Information of Triple Antibiotic

Package NDC: 0603-0644-50
Package Description: 1 TUBE in 1 CARTON (0603-0644-50) > 28.4 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 0603-0644-50
Proprietary Name Triple Antibiotic
Package Description 1 TUBE in 1 CARTON (0603-0644-50) > 28.4 g in 1 TUBE
Product NDC 0603-0644
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacitracin zinc and neomycin sulfate and polymyxin b sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19970801
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Qualitest Pharmaceuticals
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit [USP'U]/g; mg/g; [USP'U]/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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