# Divalproex Sodium

NDC: 50090-4861
Generic name: Divalproex Sodium
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20111001

FDA application: ANDA079163

## Active ingredients

- DIVALPROEX SODIUM: 125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-4861"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-4861
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c3af30e3-27ff-4285-8e4a-81856f266b32