| Product NDC: | 16590-028 |
| Proprietary Name: | BACTROBAN |
| Non Proprietary Name: | MUPIROCIN CALCIUM |
| Active Ingredient(s): | 20 mg/g & nbsp; MUPIROCIN CALCIUM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 16590-028 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050746 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980123 |
| Package NDC: | 16590-028-30 |
| Package Description: | 30 g in 1 TUBE (16590-028-30) |
| NDC Code | 16590-028-30 |
| Proprietary Name | BACTROBAN |
| Package Description | 30 g in 1 TUBE (16590-028-30) |
| Product NDC | 16590-028 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MUPIROCIN CALCIUM |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19980123 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | MUPIROCIN CALCIUM |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |