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Fluocinolone Acetonide
Fluocinolone Acetonide - 52565-012-59 - (Fluocinolone Acetonide)
Drug Information of Fluocinolone Acetonide
| Product NDC: | 52565-012 |
| 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) |
Labeler Information of Fluocinolone Acetonide
| Product NDC: | 52565-012 |
| Labeler Name: | IGI Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA015296 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20121127 |
Package Information of Fluocinolone Acetonide
| Package NDC: | 52565-012-59 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (52565-012-59) > 60 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of Fluocinolone Acetonide
| NDC Code | 52565-012-59 |
| Proprietary Name | Fluocinolone Acetonide |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (52565-012-59) > 60 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 52565-012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluocinolone Acetonide |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121127 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | IGI Labs, Inc. |
| Substance Name | FLUOCINOLONE ACETONIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
