# SODIUM ACETATE

NDC: 80830-2437
Generic name: sodium acetate
Labeler / Manufacturer: Amneal Pharmaceuticals Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20250812

FDA application: ANDA218469

## Active ingredients

- SODIUM ACETATE ANHYDROUS: 164 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80830-2437"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80830-2437
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=338105c0-c645-4b84-a125-4e1ead92b840