FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 63629-2620 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA210921
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (600 mg/1)
Marketing started20181219
Package count6

External sources

Source: openFDA. Public-domain (CC0).