# Divalproex Sodium

NDC: 55111-534
Generic name: Divalproex Sodium
Labeler / Manufacturer: Dr. Reddy's Laboratories Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130811

FDA application: ANDA090070

## 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:"55111-534"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-534
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fa823ee0-0c69-6b85-da1e-9bb2e2150ea5