# 0.9% SODIUM CHLORIDE

NDC: 51662-1520
Generic name: 0.9% SODIUM CHLORIDE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200521

FDA application: NDA016366

## Active ingredients

- SODIUM CHLORIDE: 900 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1520"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1520
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a62b71db-8ba2-6f6b-e053-2a95a90a29d1