| Product NDC: | 16590-234 |
| 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: | 16590-234 |
| Labeler Name: | STAT RX LLC USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086414 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19810409 |
| Package NDC: | 16590-234-80 |
| Package Description: | 80 g in 1 TUBE (16590-234-80) |
| NDC Code | 16590-234-80 |
| Proprietary Name | TRIAMCINOLONE ACETONIDE |
| Package Description | 80 g in 1 TUBE (16590-234-80) |
| Product NDC | 16590-234 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TRIAMCINOLONE ACETONIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19810409 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX LLC USA |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |