# Divalproex Sodium

NDC: 72789-353
Generic name: Divalproex Sodium
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20080729

FDA application: ANDA078597

## Active ingredients

- DIVALPROEX SODIUM: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-353"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-353
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90225548-85a8-4ea7-95d3-e8231c36fe5a