FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 71610-349 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryNew Drug Application (innovator) · App NDA019123
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20190621
Package count11

External sources

Source: openFDA. Public-domain (CC0).