# Divalproex sodium

NDC: 65862-595
Generic name: Divalproex sodium
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20140602

FDA application: ANDA202419

## 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:"65862-595"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-595
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6240cee7-6aa8-425c-ba46-f889a640f0fa