| Product NDC: | 67877-251 |
| 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: | 67877-251 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088042 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120401 |
| Package NDC: | 67877-251-15 |
| Package Description: | 15 g in 1 TUBE (67877-251-15) |
| NDC Code | 67877-251-15 |
| Proprietary Name | Triamcinolone Acetonide |
| Package Description | 15 g in 1 TUBE (67877-251-15) |
| Product NDC | 67877-251 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Triamcinolone Acetonide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120401 |
| Marketing Category Name | ANDA |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |