FDA NDC Directory · JSON-LD · Markdown

HYDROXYCHLOROQUINE SULFATE

NDC 42385-971 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210959
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20230306
Package count4

External sources

Source: openFDA. Public-domain (CC0).