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) |
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 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 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] |