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Hydroxychloroquine Sulfate

NDC 67046-1523 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040766
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20250224
Package count1

External sources

Source: openFDA. Public-domain (CC0).