# Sodium Chloride

NDC: 70512-841
Generic name: Sodium Chloride
Labeler / Manufacturer: SOLA Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20170525

FDA application: ANDA207956

## Active ingredients

- SODIUM CHLORIDE: 9 g/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70512-841"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70512-841
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d0bfd28-460a-48ba-bd17-cf75e56d62f4