# Divalproex Sodium

NDC: 0904-6860
Generic name: Divalproex Sodium
Labeler / Manufacturer: Major Pharmaceuticals
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-6860"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-6860
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fb39a94e-93e6-4afe-a300-f80e8f1e0fa6