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Potassium Chloride

NDC 0338-0705 · 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 (14.9 g/1000mL)
Marketing started19891226
Package count2

External sources

Source: openFDA. Public-domain (CC0).