# divalproex sodium

NDC: 68001-646
Generic name: divalproex sodium
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250606

FDA application: ANDA214643

## Active ingredients

- DIVALPROEX SODIUM: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-646"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-646
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=352b4c3c-e419-4827-9e00-febb0164e0f5