Divalproex Sodium

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Divalproex Sodium
Generic name
DIVALPROEX SODIUM
Manufacturer
Hahnemann Laboratories, INC.
Product type
HUMAN OTC DRUG
SPL set ID
f7fec516-ec6f-6248-e053-6294a90a3342
SPL ID
f7fec516-ec70-6248-e053-6294a90a3342
Version
1
Effective date
2023-03-28
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:40:41
Harmonized routes table
Harmonized routes
ORAL

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.