FDA NDC Directory · JSON-LD · Markdown

Maraviroc

NDC 68475-008 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNavinta LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217880
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMARAVIROC (150 mg/1)
Marketing started20250623
Package count1

External sources

Source: openFDA. Public-domain (CC0).