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mupirocin
mupirocin - 52125-239-01 - (Mupirocin)
Drug Information of mupirocin
| Product NDC: | 52125-239 |
| 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: | 52125-239 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065123 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130612 |
Package Information of mupirocin
| Package NDC: | 52125-239-01 |
| Package Description: | 22 g in 1 TUBE (52125-239-01) |
NDC Information of mupirocin
| NDC Code | 52125-239-01 |
| Proprietary Name | mupirocin |
| Package Description | 22 g in 1 TUBE (52125-239-01) |
| Product NDC | 52125-239 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mupirocin |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20130612 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | MUPIROCIN |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |
