# Sodium Acetate

NDC: 0641-6263
Generic name: Sodium Acetate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20240520

FDA application: ANDA216920

## 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:"0641-6263"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6263
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ee23a1c-bc99-4ff6-b2e7-d2aa42744553