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Mupirocin
Mupirocin - 68462-564-35 - (Mupirocin)
Drug Information of Mupirocin
| Product NDC: | 68462-564 |
| Proprietary Name: | Mupirocin |
| Non Proprietary Name: | Mupirocin |
| Active Ingredient(s): | 2 g/100g & nbsp; Mupirocin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mupirocin
| Product NDC: | 68462-564 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201587 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130124 |
Package Information of Mupirocin
| Package NDC: | 68462-564-35 |
| Package Description: | 30 g in 1 TUBE (68462-564-35) |
NDC Information of Mupirocin
| NDC Code | 68462-564-35 |
| Proprietary Name | Mupirocin |
| Package Description | 30 g in 1 TUBE (68462-564-35) |
| Product NDC | 68462-564 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mupirocin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130124 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | MUPIROCIN CALCIUM |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |
