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Fluocinolone Acetonide

NDC 0713-0224 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerCosette Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA089524
Dosage form / routeOINTMENT · TOPICAL
Active ingredientsFLUOCINOLONE ACETONIDE (.25 mg/g)
Marketing started19880726
Package count2

External sources

Source: openFDA. Public-domain (CC0).