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Fluocinonide
Fluocinonide - 21695-979-30 - (Fluocinonide)
Drug Information of Fluocinonide
| Product NDC: | 21695-979 |
| Proprietary Name: | Fluocinonide |
| Non Proprietary Name: | Fluocinonide |
| Active Ingredient(s): | .5 mg/g & nbsp; Fluocinonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluocinonide
| Product NDC: | 21695-979 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073481 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110120 |
Package Information of Fluocinonide
| Package NDC: | 21695-979-30 |
| Package Description: | 30 g in 1 TUBE (21695-979-30) |
NDC Information of Fluocinonide
| NDC Code | 21695-979-30 |
| Proprietary Name | Fluocinonide |
| Package Description | 30 g in 1 TUBE (21695-979-30) |
| Product NDC | 21695-979 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluocinonide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110120 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | FLUOCINONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
