Product NDC: | 54569-1544 |
Proprietary Name: | Fluocinolone Acetonide |
Non Proprietary Name: | fluocinolone acetonide |
Active Ingredient(s): | .1 mg/g & nbsp; fluocinolone acetonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1544 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088170 |
Marketing Category: | ANDA |
Start Marketing Date: | 19821216 |
Package NDC: | 54569-1544-0 |
Package Description: | 15 g in 1 TUBE (54569-1544-0) |
NDC Code | 54569-1544-0 |
Proprietary Name | Fluocinolone Acetonide |
Package Description | 15 g in 1 TUBE (54569-1544-0) |
Product NDC | 54569-1544 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluocinolone acetonide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19821216 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | FLUOCINOLONE ACETONIDE |
Strength Number | .1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |