FDA NDC Directory · JSON-LD · Markdown

Hydroxychloroquine Sulfate

NDC 71335-3079 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA040766
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (200 mg/1)
Marketing started20240603
Package count9

External sources

Source: openFDA. Public-domain (CC0).