# Depakote ER

NDC: 0074-7401
Generic name: Divalproex Sodium
Labeler / Manufacturer: AbbVie Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20000804

FDA application: NDA021168

## 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:"0074-7401"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0074-7401
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0dc024ce-efc8-4690-7cb5-639c728fccac