# Divalproex Sodium

NDC: 68084-313
Generic name: Divalproex Sodium
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, COATED PELLETS
Routes: ORAL
Marketing started: 20090318

FDA application: ANDA078919

## 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:"68084-313"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-313
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e4778d8-8798-4da1-bb33-1aa1414b5809