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Potassium Chloride Extended-Release

NDC 63304-076 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namePotassium Chloride
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076368
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20191120
Package count3

External sources

Source: openFDA. Public-domain (CC0).