| Product NDC: | 0168-0059 |
| 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: | 0168-0059 |
| Labeler Name: | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088167 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19821216 |
| Package NDC: | 0168-0059-60 |
| Package Description: | 60 mL in 1 BOTTLE (0168-0059-60) |
| NDC Code | 0168-0059-60 |
| Proprietary Name | Fluocinolone Acetonide |
| Package Description | 60 mL in 1 BOTTLE (0168-0059-60) |
| Product NDC | 0168-0059 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluocinolone acetonide |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19821216 |
| Marketing Category Name | ANDA |
| Labeler Name | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
| Substance Name | FLUOCINOLONE ACETONIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |