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POTASSIUM CHLORIDE

NDC 72888-099 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAdvagen Pharma Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA216321
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1500 mg/1)
Marketing started20230616
Package count2

External sources

Source: openFDA. Public-domain (CC0).