FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 0603-1542 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA206814
Dosage form / routeSOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (20 meq/15mL)
Marketing started20150504
Marketing ended20260930
Package count1

External sources

Source: openFDA. Public-domain (CC0).