BACiiM - 39822-0277-5 - (Bacitracin)

Alphabetical Index


Drug Information of BACiiM

Product NDC: 39822-0277
Proprietary Name: BACiiM
Non Proprietary Name: Bacitracin
Active Ingredient(s): 50000    [USP'U]/1 & nbsp;   Bacitracin
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BACiiM

Product NDC: 39822-0277
Labeler Name: X-GEN Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064153
Marketing Category: ANDA
Start Marketing Date: 19970509

Package Information of BACiiM

Package NDC: 39822-0277-5
Package Description: 10 VIAL in 1 CARTON (39822-0277-5) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0277-2)

NDC Information of BACiiM

NDC Code 39822-0277-5
Proprietary Name BACiiM
Package Description 10 VIAL in 1 CARTON (39822-0277-5) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0277-2)
Product NDC 39822-0277
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bacitracin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 19970509
Marketing Category Name ANDA
Labeler Name X-GEN Pharmaceuticals, Inc.
Substance Name BACITRACIN
Strength Number 50000
Strength Unit [USP'U]/1
Pharmaceutical Classes Decreased Cell Wall Synthesis & Repair [PE]

Complete Information of BACiiM


General Information