# divalproex sodium

NDC: 29300-381
Generic name: divalproex sodium
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220225

FDA application: ANDA214643

## Active ingredients

- DIVALPROEX SODIUM: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-381"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-381
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d4129ae-0ce8-4a04-9f9d-c770508de8ed