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Potassium Chloride

NDC 59651-429 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214728
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20210331
Package count3

External sources

Source: openFDA. Public-domain (CC0).