bacitracin - 37808-536-64 - (Bacitracin)

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Drug Information of bacitracin

Product NDC: 37808-536
Proprietary Name: bacitracin
Non Proprietary Name: Bacitracin
Active Ingredient(s): 500    [USP'U]/g & nbsp;   Bacitracin
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of bacitracin

Product NDC: 37808-536
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19910615

Package Information of bacitracin

Package NDC: 37808-536-64
Package Description: 1 TUBE in 1 CARTON (37808-536-64) > 28 g in 1 TUBE

NDC Information of bacitracin

NDC Code 37808-536-64
Proprietary Name bacitracin
Package Description 1 TUBE in 1 CARTON (37808-536-64) > 28 g in 1 TUBE
Product NDC 37808-536
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19910615
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name BACITRACIN
Strength Number 500
Strength Unit [USP'U]/g
Pharmaceutical Classes

Complete Information of bacitracin


General Information