FDA NDC Directory · JSON-LD · Markdown

HYDROXYCHLOROQUINE SULFATE

NDC 82619-131 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namehydroxychloroquine sulfate
Labeler / ManufacturerCreekwood Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040150
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20250508
Package count3

External sources

Source: openFDA. Public-domain (CC0).