Product NDC: | 42254-176 |
Proprietary Name: | triamcinolone acetonide |
Non Proprietary Name: | triamcinolone acetonide |
Active Ingredient(s): | .25 mg/g & nbsp; triamcinolone acetonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42254-176 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085691 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091007 |
Package NDC: | 42254-176-80 |
Package Description: | 80 g in 1 TUBE (42254-176-80) |
NDC Code | 42254-176-80 |
Proprietary Name | triamcinolone acetonide |
Package Description | 80 g in 1 TUBE (42254-176-80) |
Product NDC | 42254-176 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | triamcinolone acetonide |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20091007 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | TRIAMCINOLONE ACETONIDE |
Strength Number | .25 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |