FDA NDC Directory · JSON-LD · Markdown

Desonide

NDC 51672-4079 · HUMAN PRESCRIPTION DRUG · LOTION

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202161
Dosage form / routeLOTION · TOPICAL
Active ingredientsDESONIDE (.5 mg/mL)
Marketing started20141031
Package count2

External sources

Source: openFDA. Public-domain (CC0).