FDA NDC Directory · JSON-LD · Markdown

SODIUM CHLORIDE

NDC 51662-1464 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryNew Drug Application (innovator) · App NDA018803
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsSODIUM CHLORIDE (9 mg/mL)
Marketing started20191212
Package count1

External sources

Source: openFDA. Public-domain (CC0).