# Divalproex Sodium

NDC: 0074-7345
Generic name: Divalproex Sodium
Labeler / Manufacturer: AbbVie Inc.
Product type: DRUG FOR FURTHER PROCESSING
Marketing category: DRUG FOR FURTHER PROCESSING
Dosage form: TABLET, DELAYED RELEASE
Routes: —
Marketing started: 20260922



## Active ingredients

- DIVALPROEX SODIUM: 125 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0074-7345"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0074-7345