Product NDC: | 68788-9172 |
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: | 68788-9172 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA086414 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060928 |
Package NDC: | 68788-9172-8 |
Package Description: | 1 TUBE in 1 CARTON (68788-9172-8) > 80 g in 1 TUBE |
NDC Code | 68788-9172-8 |
Proprietary Name | Triamcinolone Acetonide |
Package Description | 1 TUBE in 1 CARTON (68788-9172-8) > 80 g in 1 TUBE |
Product NDC | 68788-9172 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Triamcinolone Acetonide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20060928 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | TRIAMCINOLONE ACETONIDE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |