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Mupirocin
Mupirocin - 50436-0025-1 - (mupirocin)
Drug Information of Mupirocin
| Product NDC: | 50436-0025 |
| 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: | 50436-0025 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065192 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20051130 |
Package Information of Mupirocin
| Package NDC: | 50436-0025-1 |
| Package Description: | 22 g in 1 BOTTLE (50436-0025-1) |
NDC Information of Mupirocin
| NDC Code | 50436-0025-1 |
| Proprietary Name | Mupirocin |
| Package Description | 22 g in 1 BOTTLE (50436-0025-1) |
| Product NDC | 50436-0025 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mupirocin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20051130 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | MUPIROCIN |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |
