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Fluocinolone Acetonide
Fluocinolone Acetonide - 0713-0222-60 - (Fluocinolone Acetonide)
Drug Information of Fluocinolone Acetonide
| Product NDC: | 0713-0222 |
| Proprietary Name: | Fluocinolone Acetonide |
| Non Proprietary Name: | Fluocinolone Acetonide |
| Active Ingredient(s): | .25 mg/g & nbsp; Fluocinolone Acetonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluocinolone Acetonide
| Product NDC: | 0713-0222 |
| Labeler Name: | GW Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089525 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880726 |
Package Information of Fluocinolone Acetonide
| Package NDC: | 0713-0222-60 |
| Package Description: | 60 g in 1 TUBE (0713-0222-60) |
NDC Information of Fluocinolone Acetonide
| NDC Code | 0713-0222-60 |
| Proprietary Name | Fluocinolone Acetonide |
| Package Description | 60 g in 1 TUBE (0713-0222-60) |
| Product NDC | 0713-0222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluocinolone Acetonide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19880726 |
| Marketing Category Name | ANDA |
| Labeler Name | GW Laboratories, Inc. |
| Substance Name | FLUOCINOLONE ACETONIDE |
| Strength Number | .25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
