United States · FDA National Drug Code directory

Divalproex sodium

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 72162-2516_f88bd40f-33f3-41a2-b271-7f031b3c7fd7
Product NDC: 72162-2516
Form: TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term: Divalproex sodium
Labeler: Bryant Ranch Prepack
Marketing category: ANDA
Marketing start / end (source format): 20140602
Source listing expiry: 20261231

Source-listed ingredients

DIVALPROEX SODIUM — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-1) · 72162-2516-1
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-5) · 72162-2516-5

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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