| Product NDC: | 0168-0089 |
| 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) |
| Product NDC: | 0168-0089 |
| Labeler Name: | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062602 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19851009 |
| Package NDC: | 0168-0089-30 |
| Package Description: | 30 g in 1 TUBE (0168-0089-30) |
| NDC Code | 0168-0089-30 |
| Proprietary Name | Nystatin and Triamcinolone Acetonide |
| Package Description | 30 g in 1 TUBE (0168-0089-30) |
| Product NDC | 0168-0089 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nystatin and triamcinolone acetonide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19851009 |
| Marketing Category Name | ANDA |
| Labeler Name | E. FOUGERA & CO., A division of Fougera Pharmaceuticals 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] |