# Divalproex Sodium

NDC: 0904-6363
Generic name: Divalproex Sodium
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130811

FDA application: ANDA090161

## Active ingredients

- DIVALPROEX SODIUM: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-6363"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-6363
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4ef6c5fd-42b2-4419-9b5a-e6d63571e3a0