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: | 67877-251-80 |
Package Description: | 80 g in 1 TUBE (67877-251-80) |
NDC Code | 67877-251-80 |
Proprietary Name | Triamcinolone Acetonide |
Package Description | 80 g in 1 TUBE (67877-251-80) |
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 |