# Divalproex Sodium

NDC: 68084-415
Generic name: Divalproex Sodium
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20131121
Marketing ended: 20261130
FDA application: ANDA078239

## Active ingredients

- DIVALPROEX SODIUM: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68084-415"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-415
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8ba3986-1ded-44a8-8d10-d0f252a07794