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Rilpivirine

NDC 70069-848 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218798
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRILPIVIRINE HYDROCHLORIDE (25 mg/1)
Marketing started20260130
Package count1

External sources

Source: openFDA. Public-domain (CC0).