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SOVUNA

NDC 70954-804 · 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 (200 mg/1)
Marketing started20230915
Package count3

External sources

Source: openFDA. Public-domain (CC0).