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Maraviroc

NDC 68554-3080 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerHetero Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203347
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMARAVIROC (300 mg/1)
Marketing started20220206
Package count1

External sources

Source: openFDA. Public-domain (CC0).