FDA NDC Directory · JSON-LD · Markdown

Desonide

NDC 0472-0803 · HUMAN PRESCRIPTION DRUG · LOTION

Generic namedesonide
Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA072354
Dosage form / routeLOTION · TOPICAL
Active ingredientsDESONIDE (.5 mg/mL)
Marketing started20090528
Marketing ended20280331
Package count2

External sources

Source: openFDA. Public-domain (CC0).