| Product NDC: | 52959-652 |
| Proprietary Name: | Fluocinonide |
| Non Proprietary Name: | Fluocinonide |
| Active Ingredient(s): | .5 mg/g & nbsp; Fluocinonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52959-652 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072537 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110120 |
| Package NDC: | 52959-652-60 |
| Package Description: | 60 g in 1 TUBE (52959-652-60) |
| NDC Code | 52959-652-60 |
| Proprietary Name | Fluocinonide |
| Package Description | 60 g in 1 TUBE (52959-652-60) |
| Product NDC | 52959-652 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluocinonide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110120 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | FLUOCINONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |