# Divalproex Sodium

NDC: 63187-742
Generic name: Divalproex Sodium
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20111001

FDA application: ANDA079163

## Active ingredients

- DIVALPROEX SODIUM: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-742"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-742
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=abac11e6-7ce1-491c-9ac3-61f3df54c4a4