# Divalproex Sodium

NDC: 55154-7145
Generic name: Divalproex Sodium
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20150302
Marketing ended: 20260630
FDA application: ANDA090554

## 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:"55154-7145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-7145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee2e8924-2379-400d-9895-e3aa02fe6426