# Divalproex sodium

NDC: 16714-484
Generic name: Divalproex sodium
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20140602

FDA application: ANDA202419

## 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:"16714-484"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-484
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aab6b411-11e9-4a16-afb6-d471ba4756e9