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Potassium Chloride

NDC 0378-4560 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namepotassium chloride
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204662
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (8 meq/1)
Marketing started20161109
Marketing ended20261231
Package count2

External sources

Source: openFDA. Public-domain (CC0).