FDA NDC Directory · JSON-LD · Markdown

SOVUNA

NDC 70954-805 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameHydroxychloroquine Sulfate
Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA214581
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsHYDROXYCHLOROQUINE SULFATE (300 mg/1)
Marketing started20230915
Package count2

External sources

Source: openFDA. Public-domain (CC0).