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KLOR-CON

NDC 0245-0835 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namepotassium chloride
Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218979
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (600 mg/1)
Marketing started20250815
Package count2

External sources

Source: openFDA. Public-domain (CC0).