FDA NDC Directory · JSON-LD · Markdown

POTASSIUM CHLORIDE

NDC 0409-6635 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA080205
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsPOTASSIUM CHLORIDE (149 mg/mL)
Marketing started20050919
Package count1

External sources

Source: openFDA. Public-domain (CC0).