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Primaquine Phosphate

NDC 0024-1596 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSanofi-Aventis U.S. LLC
Marketing categoryNew Drug Application (innovator) · App NDA008316
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRIMAQUINE PHOSPHATE (15 mg/1)
Marketing started20110415
Package count1

External sources

Source: openFDA. Public-domain (CC0).