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Hydroxychloroquine sulfate

NDC 71335-0897 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA040657
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20080103
Package count9

External sources

Source: openFDA. Public-domain (CC0).