FDA NDC Directory · JSON-LD · Markdown

Hydroxychloroquine sulfate

NDC 57664-761 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201691
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20180618
Package count2

External sources

Source: openFDA. Public-domain (CC0).