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Primaquine Phosphate

NDC 76385-102 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204476
Dosage form / routeTABLET · ORAL
Active ingredientsPRIMAQUINE PHOSPHATE (15 mg/1)
Marketing started20140801
Package count1

External sources

Source: openFDA. Public-domain (CC0).