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] |