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Potassium Chloride

NDC 64380-861 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA210733
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20181127
Package count3

External sources

Source: openFDA. Public-domain (CC0).