# Divalproex sodium

NDC: 31722-021
Generic name: Divalproex sodium
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230923

FDA application: ANDA215527

## Active ingredients

- DIVALPROEX SODIUM: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8e954d4-54e3-491c-867c-b3b656b70f23