FDA NDC Directory · JSON-LD · Markdown

POTASSIUM CHLORIDE

NDC 59651-959 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic namePotassium Chloride
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216536
Dosage form / routeSOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (20 meq/15mL)
Marketing started20251120
Package count1

External sources

Source: openFDA. Public-domain (CC0).