# divalproex sodium

NDC: 60687-904
Generic name: divalproex sodium
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20251218

FDA application: ANDA214643

## 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:"60687-904"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-904
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b12b76a0-4b6e-4cd4-9508-10a2c84d8beb