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Potassium Chloride

NDC 62037-720 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075604
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (20 meq/1)
Marketing started20020410
Marketing ended20270430
Package count3

External sources

Source: openFDA. Public-domain (CC0).