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MUPIROCIN
MUPIROCIN - 16590-158-22 - (MUPIROCIN)
Drug Information of MUPIROCIN
| Product NDC: | 16590-158 |
| Proprietary Name: | MUPIROCIN |
| Non Proprietary Name: | MUPIROCIN |
| Active Ingredient(s): | 20 mg/g & nbsp; MUPIROCIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MUPIROCIN
| Product NDC: | 16590-158 |
| Labeler Name: | STAT RX LLC USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065123 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031107 |
Package Information of MUPIROCIN
| Package NDC: | 16590-158-22 |
| Package Description: | 22 g in 1 TUBE (16590-158-22) |
NDC Information of MUPIROCIN
| NDC Code | 16590-158-22 |
| Proprietary Name | MUPIROCIN |
| Package Description | 22 g in 1 TUBE (16590-158-22) |
| Product NDC | 16590-158 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MUPIROCIN |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20031107 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX LLC USA |
| Substance Name | MUPIROCIN |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |
