Bacitracin - 0009-0233-03 - (Bacitracin)

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Drug Information of Bacitracin

Product NDC: 0009-0233
Proprietary Name: Bacitracin
Non Proprietary Name: Bacitracin
Active Ingredient(s): 50000    [iU]/1 & nbsp;   Bacitracin
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bacitracin

Product NDC: 0009-0233
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060733
Marketing Category: ANDA
Start Marketing Date: 19480729

Package Information of Bacitracin

Package NDC: 0009-0233-03
Package Description: 10 VIAL in 1 CARTON (0009-0233-03) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Bacitracin

NDC Code 0009-0233-03
Proprietary Name Bacitracin
Package Description 10 VIAL in 1 CARTON (0009-0233-03) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 0009-0233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bacitracin
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 19480729
Marketing Category Name ANDA
Labeler Name Pharmacia and Upjohn Company
Substance Name BACITRACIN
Strength Number 50000
Strength Unit [iU]/1
Pharmaceutical Classes Decreased Cell Wall Synthesis & Repair [PE]

Complete Information of Bacitracin


General Information