# Divalproex Sodium

NDC: 71610-032
Generic name: Divalproex Sodium
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20140321

FDA application: ANDA078182

## Active ingredients

- DIVALPROEX SODIUM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-032"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-032
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9cfdcb58-d6d7-43bb-b6e1-17172b143296