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Potassium Chloride Extended-release

NDC 70010-135 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214452
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1500 mg/1)
Marketing started20210130
Package count3

External sources

Source: openFDA. Public-domain (CC0).