FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 0832-5324 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namepotassium chloride
Labeler / ManufacturerUpsher-SmithLaboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074726
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started19981120
Package count2

External sources

Source: openFDA. Public-domain (CC0).