Product NDC: | 64980-320 |
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): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64980-320 |
Labeler Name: | Rising Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040771 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100707 |
Package NDC: | 64980-320-05 |
Package Description: | 48 CARTON in 1 BOX (64980-320-05) > 1 TUBE in 1 CARTON > 5 g in 1 TUBE |
NDC Code | 64980-320-05 |
Proprietary Name | Triamcinolone Acetonide |
Package Description | 48 CARTON in 1 BOX (64980-320-05) > 1 TUBE in 1 CARTON > 5 g in 1 TUBE |
Product NDC | 64980-320 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Triamcinolone Acetonide |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20100707 |
Marketing Category Name | ANDA |
Labeler Name | Rising Pharmaceuticals, Inc. |
Substance Name | TRIAMCINOLONE ACETONIDE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |