Product NDC: | 21695-185 |
Proprietary Name: | Nystatin and Triamcinolone |
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): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-185 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062364 |
Marketing Category: | ANDA |
Start Marketing Date: | 19871222 |
Package NDC: | 21695-185-15 |
Package Description: | 15 g in 1 TUBE (21695-185-15) |
NDC Code | 21695-185-15 |
Proprietary Name | Nystatin and Triamcinolone |
Package Description | 15 g in 1 TUBE (21695-185-15) |
Product NDC | 21695-185 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nystatin and Triamcinolone Acetonide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19871222 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | NYSTATIN; TRIAMCINOLONE ACETONIDE |
Strength Number | 100000; 1 |
Strength Unit | [USP'U]/g; mg/g |
Pharmaceutical Classes | Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |