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Bacitracin
Bacitracin - 63323-329-31 - (BACITRACIN)
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] |
