Bacitracin - 67777-219-05 - (Bacitracin)

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Drug Information of Bacitracin

Product NDC: 67777-219
Proprietary Name: Bacitracin
Non Proprietary Name: Bacitracin
Active Ingredient(s): 500    [iU]/g & nbsp;   Bacitracin
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Bacitracin

Product NDC: 67777-219
Labeler Name: Dynarex Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091201

Package Information of Bacitracin

Package NDC: 67777-219-05
Package Description: 72 TUBE in 1 CASE (67777-219-05) > 56.7 g in 1 TUBE

NDC Information of Bacitracin

NDC Code 67777-219-05
Proprietary Name Bacitracin
Package Description 72 TUBE in 1 CASE (67777-219-05) > 56.7 g in 1 TUBE
Product NDC 67777-219
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20091201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dynarex Corporation
Substance Name BACITRACIN
Strength Number 500
Strength Unit [iU]/g
Pharmaceutical Classes

Complete Information of Bacitracin


General Information