# sodium chloride

NDC: 64253-202
Generic name: SODIUM CHLORIDE
Labeler / Manufacturer: Medefil, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20120113

FDA application: NDA202832

## Active ingredients

- SODIUM CHLORIDE: 9 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64253-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64253-202
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1468c0f-dd4f-4d38-a84c-c1d110303965