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POTASSIUM CHLORIDE

NDC 65219-008 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211087
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsPOTASSIUM CHLORIDE (20 meq/50mL)
Marketing started20210625
Package count1

External sources

Source: openFDA. Public-domain (CC0).