| Product NDC: | 0603-7862 |
| 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: | 0603-7862 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040671 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060609 |
| Package NDC: | 0603-7862-74 |
| Package Description: | 15 g in 1 TUBE (0603-7862-74) |
| NDC Code | 0603-7862-74 |
| Proprietary Name | Triamcinolone Acetonide |
| Package Description | 15 g in 1 TUBE (0603-7862-74) |
| Product NDC | 0603-7862 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | triamcinolone acetonide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20060609 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |