FDA NDC Directory · JSON-LD · Markdown

PRIMAQUINE PHOSPHATE

NDC 50742-191 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206043
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRIMAQUINE PHOSPHATE (15 mg/1)
Marketing started20180123
Package count2

External sources

Source: openFDA. Public-domain (CC0).