# Divalproex Sodium

NDC: 55154-5633
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: 20140321
Marketing ended: 20270831
FDA application: ANDA078182

## Active ingredients

- DIVALPROEX SODIUM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55154-5633"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-5633
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4fc50afb-67f3-4bf3-9ec3-cc12734f47fd