# Sodium Acetate

NDC: 0409-7299
Generic name: SODIUM ACETATE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20140305

FDA application: NDA018893

## Active ingredients

- SODIUM ACETATE ANHYDROUS: 3.28 g/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-7299"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-7299
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce9a7469-c4ba-4f60-8f7a-47ef0974316e