# divalproex sodium

NDC: 69452-435
Generic name: divalproex sodium
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20240626

FDA application: ANDA078853

## Active ingredients

- DIVALPROEX SODIUM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69452-435"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-435
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19064624-81d1-4ce3-bfe4-955bad6af6a2