# DIVALPROEX SODIUM

NDC: 61919-249
Generic name: divalproex sodium
Labeler / Manufacturer: DirectRx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20220406

FDA application: ANDA079163

## 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:"61919-249"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-249
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce12c7b1-caa9-4224-bb5f-3e20e0281d66