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: 29300-140_8e888ed9-2d55-4e95-ba7b-8b437481c947
Product NDC: 29300-140
Form: TABLET, DELAYED RELEASE
Composition / generic term: Divalproex Sodium
Labeler: Unichem Pharmaceuticals (USA), Inc.
Marketing category: ANDA
Marketing start / end (source format): 20111001
Source listing expiry: 20271231

Source-listed ingredients

DIVALPROEX SODIUM — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-01) · 29300-140-01
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-05) · 29300-140-05
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-10) · 29300-140-10

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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