FDA NDC Directory · JSON-LD · Markdown

Mometasone Furoate

NDC 68462-385 · HUMAN PRESCRIPTION DRUG · LOTION

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA090506
Dosage form / routeLOTION · TOPICAL
Active ingredientsMOMETASONE FUROATE (1 mg/mL)
Marketing started20200601
Package count2

External sources

Source: openFDA. Public-domain (CC0).