| Product NDC: | 49999-172 |
| Proprietary Name: | Fluocinonide |
| Non Proprietary Name: | Fluocinonide |
| Active Ingredient(s): | .5 mg/g & nbsp; Fluocinonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49999-172 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019117 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19840626 |
| Package NDC: | 49999-172-15 |
| Package Description: | 1 TUBE in 1 CARTON (49999-172-15) > 15 g in 1 TUBE |
| NDC Code | 49999-172-15 |
| Proprietary Name | Fluocinonide |
| Package Description | 1 TUBE in 1 CARTON (49999-172-15) > 15 g in 1 TUBE |
| Product NDC | 49999-172 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluocinonide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19840626 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | FLUOCINONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |