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Potassium Chloride

NDC 0832-5322 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryNew Drug Application (innovator) · App NDA019123
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (600 mg/1)
Marketing started19860417
Package count2

External sources

Source: openFDA. Public-domain (CC0).