Product NDC: | 0093-0264 |
Proprietary Name: | Fluocinonide |
Non Proprietary Name: | Fluocinonide |
Active Ingredient(s): | .5 mg/g & nbsp; Fluocinonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0093-0264 |
Labeler Name: | Teva Pharmaceuticals USA Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA073481 |
Marketing Category: | ANDA |
Start Marketing Date: | 19920501 |
Package NDC: | 0093-0264-15 |
Package Description: | 15 g in 1 TUBE (0093-0264-15) |
NDC Code | 0093-0264-15 |
Proprietary Name | Fluocinonide |
Package Description | 15 g in 1 TUBE (0093-0264-15) |
Product NDC | 0093-0264 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluocinonide |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19920501 |
Marketing Category Name | ANDA |
Labeler Name | Teva Pharmaceuticals USA Inc |
Substance Name | FLUOCINONIDE |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |