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Nystatin and Triamcinolone Acetonide
Nystatin and Triamcinolone Acetonide - 51672-1272-1 - (Nystatin and Triamcinolone Acetonide)
Drug Information of Nystatin and Triamcinolone Acetonide
| Product NDC: | 51672-1272 |
| Proprietary Name: | Nystatin and Triamcinolone Acetonide |
| Non Proprietary Name: | Nystatin and Triamcinolone Acetonide |
| Active Ingredient(s): | 100000; 1 [USP'U]/g; mg/g & nbsp; Nystatin and Triamcinolone Acetonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nystatin and Triamcinolone Acetonide
| Product NDC: | 51672-1272 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063305 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930329 |
Package Information of Nystatin and Triamcinolone Acetonide
| Package NDC: | 51672-1272-1 |
| Package Description: | 1 TUBE in 1 CARTON (51672-1272-1) > 15 g in 1 TUBE |
NDC Information of Nystatin and Triamcinolone Acetonide
| NDC Code | 51672-1272-1 |
| Proprietary Name | Nystatin and Triamcinolone Acetonide |
| Package Description | 1 TUBE in 1 CARTON (51672-1272-1) > 15 g in 1 TUBE |
| Product NDC | 51672-1272 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nystatin and Triamcinolone Acetonide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19930329 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | NYSTATIN; TRIAMCINOLONE ACETONIDE |
| Strength Number | 100000; 1 |
| Strength Unit | [USP'U]/g; mg/g |
| Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
