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Potassium Chloride

NDC 60760-423 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerSt. Mary's Medical Park Pharmacy
Marketing categoryAbbreviated NDA (generic) · App ANDA209314
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20260619
Package count1

External sources

Source: openFDA. Public-domain (CC0).