| Product NDC: | 66993-942 |
| Proprietary Name: | Mupirocin Calcium |
| 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: | 66993-942 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050746 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130128 |
| Package NDC: | 66993-942-31 |
| Package Description: | 1 TUBE in 1 CARTON (66993-942-31) > 30 g in 1 TUBE |
| NDC Code | 66993-942-31 |
| Proprietary Name | Mupirocin Calcium |
| Package Description | 1 TUBE in 1 CARTON (66993-942-31) > 30 g in 1 TUBE |
| Product NDC | 66993-942 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mupirocin calcium |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130128 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Prasco Laboratories |
| Substance Name | MUPIROCIN CALCIUM |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA] |