# divalproex sodium

NDC: 67046-1683
Generic name: divalproex sodium
Labeler / Manufacturer: Coupler LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260706

FDA application: ANDA078853

## 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:"67046-1683"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67046-1683
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55f1614b-aadc-34ca-e063-6394a90ae2a7