FDA NDC Directory · JSON-LD · Markdown

SODIUM CHLORIDE

NDC 0409-1141 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerHospira, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018897
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM CHLORIDE (234 mg/mL)
Marketing started20050430
Package count1

External sources

Source: openFDA. Public-domain (CC0).