BACITRACIN - 48102-007-13 - (BACITRACIN)

Alphabetical Index


Drug Information of BACITRACIN

Product NDC: 48102-007
Proprietary Name: BACITRACIN
Non Proprietary Name: BACITRACIN
Active Ingredient(s): 500    [iU]/g & nbsp;   BACITRACIN
Administration Route(s): OPHTHALMIC
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of BACITRACIN

Product NDC: 48102-007
Labeler Name: Fera Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061212
Marketing Category: ANDA
Start Marketing Date: 20100111

Package Information of BACITRACIN

Package NDC: 48102-007-13
Package Description: 3 TUBE in 1 CARTON (48102-007-13) > 1 g in 1 TUBE (48102-007-11)

NDC Information of BACITRACIN

NDC Code 48102-007-13
Proprietary Name BACITRACIN
Package Description 3 TUBE in 1 CARTON (48102-007-13) > 1 g in 1 TUBE (48102-007-11)
Product NDC 48102-007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BACITRACIN
Dosage Form Name OINTMENT
Route Name OPHTHALMIC
Start Marketing Date 20100111
Marketing Category Name ANDA
Labeler Name Fera Pharmaceuticals
Substance Name BACITRACIN
Strength Number 500
Strength Unit [iU]/g
Pharmaceutical Classes Decreased Cell Wall Synthesis & Repair [PE]

Complete Information of BACITRACIN


General Information