FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 0338-0709 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namePOTASSIUM CHLORIDE
Labeler / ManufacturerBaxter Healthcare Corporation
Marketing categoryNew Drug Application (innovator) · App NDA019904
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsPOTASSIUM CHLORIDE (7.46 g/1000mL)
Marketing started19891226
Package count1

External sources

Source: openFDA. Public-domain (CC0).