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POTASSIUM CHLORIDE EXTENDED RELEASE

NDC 70010-022 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namePOTASSIUM CHLORIDE
Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211797
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20201022
Package count5

External sources

Source: openFDA. Public-domain (CC0).