FDA NDC Directory · JSON-LD · Markdown

HYDROXYCHLOROQUINE SULFATE

NDC 59651-889 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA040274
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20250307
Package count2

External sources

Source: openFDA. Public-domain (CC0).