| Product NDC: | 55154-4522 |
| Proprietary Name: | BACTROBAN |
| Non Proprietary Name: | mupirocin calcium |
| Active Ingredient(s): | 20 mg/g & nbsp; mupirocin calcium |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-4522 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050703 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960410 |
| Package NDC: | 55154-4522-5 |
| Package Description: | 5 TUBE in 1 BAG (55154-4522-5) > 1 g in 1 TUBE |
| NDC Code | 55154-4522-5 |
| Proprietary Name | BACTROBAN |
| Package Description | 5 TUBE in 1 BAG (55154-4522-5) > 1 g in 1 TUBE |
| Product NDC | 55154-4522 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mupirocin calcium |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19960410 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | MUPIROCIN CALCIUM |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |