Bacitracin - 63323-329-31 - (BACITRACIN)

Alphabetical Index


Drug Information of Bacitracin

Product NDC: 63323-329
Proprietary Name: Bacitracin
Non Proprietary Name: BACITRACIN
Active Ingredient(s): 50000    [iU]/1 & nbsp;   BACITRACIN
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bacitracin

Product NDC: 63323-329
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065116
Marketing Category: ANDA
Start Marketing Date: 20030128

Package Information of Bacitracin

Package NDC: 63323-329-31
Package Description: 10 VIAL in 1 CARTON (63323-329-31) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Bacitracin

NDC Code 63323-329-31
Proprietary Name Bacitracin
Package Description 10 VIAL in 1 CARTON (63323-329-31) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 63323-329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BACITRACIN
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 20030128
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name BACITRACIN
Strength Number 50000
Strength Unit [iU]/1
Pharmaceutical Classes Decreased Cell Wall Synthesis & Repair [PE]

Complete Information of Bacitracin


General Information