FDA NDC Directory · JSON-LD · Markdown

POTASSIUM CHLORIDE EXTENDED RELEASE

NDC 16571-842 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namepotassium chloride
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217412
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (600 mg/1)
Marketing started20250213
Package count3

External sources

Source: openFDA. Public-domain (CC0).