Product NDC: | 54868-2264 |
Proprietary Name: | Fluocinolone Acetonide |
Non Proprietary Name: | fluocinolone acetonide |
Active Ingredient(s): | .1 mg/mL & nbsp; fluocinolone acetonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-2264 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088167 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960403 |
Package NDC: | 54868-2264-1 |
Package Description: | 1 BOTTLE in 1 CARTON (54868-2264-1) > 60 mL in 1 BOTTLE |
NDC Code | 54868-2264-1 |
Proprietary Name | Fluocinolone Acetonide |
Package Description | 1 BOTTLE in 1 CARTON (54868-2264-1) > 60 mL in 1 BOTTLE |
Product NDC | 54868-2264 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluocinolone acetonide |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19960403 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | FLUOCINOLONE ACETONIDE |
Strength Number | .1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |