Product NDC: | 21695-189 |
Proprietary Name: | Triamcinolone Acetonide |
Non Proprietary Name: | Triamcinolone Acetonide |
Active Ingredient(s): | 1 mg/g & nbsp; Triamcinolone Acetonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-189 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085692 |
Marketing Category: | ANDA |
Start Marketing Date: | 19780309 |
Package NDC: | 21695-189-15 |
Package Description: | 15 g in 1 TUBE (21695-189-15) |
NDC Code | 21695-189-15 |
Proprietary Name | Triamcinolone Acetonide |
Package Description | 15 g in 1 TUBE (21695-189-15) |
Product NDC | 21695-189 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Triamcinolone Acetonide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19780309 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | TRIAMCINOLONE ACETONIDE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |