| 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: | 67877-251-30 | 
| Package Description: | 30 g in 1 TUBE (67877-251-30) | 
| NDC Code | 67877-251-30 | 
| Proprietary Name | Triamcinolone Acetonide | 
| Package Description | 30 g in 1 TUBE (67877-251-30) | 
| 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 |