Product NDC: | 0168-0004 |
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: | 0168-0004 |
Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085692 |
Marketing Category: | ANDA |
Start Marketing Date: | 19780309 |
Package NDC: | 0168-0004-80 |
Package Description: | 1 TUBE in 1 CARTON (0168-0004-80) > 80 g in 1 TUBE |
NDC Code | 0168-0004-80 |
Proprietary Name | triamcinolone acetonide |
Package Description | 1 TUBE in 1 CARTON (0168-0004-80) > 80 g in 1 TUBE |
Product NDC | 0168-0004 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | triamcinolone acetonide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19780309 |
Marketing Category Name | ANDA |
Labeler Name | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
Substance Name | TRIAMCINOLONE ACETONIDE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes |