# Valproate Sodium

NDC: 63323-494
Generic name: VALPROATE SODIUM
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20030818

FDA application: ANDA076539

## Active ingredients

- VALPROATE SODIUM: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-494"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-494
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3dfb6da1-f66a-4618-9f74-d2d6c16c0b58