# Divalproex sodium

NDC: 70518-3457
Generic name: Divalproex sodium
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, COATED PELLETS
Routes: ORAL
Marketing started: 20200720

FDA application: ANDA213181

## 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:"70518-3457"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3457
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ead614c-a68d-4a2f-94d0-e6404a8f8760