# Divalproex sodium

NDC: 71610-157
Generic name: Divalproex sodium
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
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: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-157"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-157
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ad5e8bd8-c923-40f0-a106-55620c4247d7