FDA NDC Directory · JSON-LD · Markdown

Sotalol Hydrochloride

NDC 69584-844 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerOxford Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075563
Dosage form / routeTABLET · ORAL
Active ingredientsSOTALOL HYDROCHLORIDE (240 mg/1)
Marketing started20200724
Package count1

External sources

Source: openFDA. Public-domain (CC0).