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Potassium Chloride

NDC 63739-972 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namepotassium chloride
Labeler / ManufacturerMckesson Corporation DBA SKY Packaginng
Marketing categoryAbbreviated NDA (generic) · App ANDA074726
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started19981120
Marketing ended20260831
Package count1

External sources

Source: openFDA. Public-domain (CC0).