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PACK IN HAND · ONE-PAGE CHECK

Medicine pack check sheet

Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.

Published record starting point

Record display name
DEPAKOTE
Generic name / active ingredient
divalproex sodium delayed-release tablets
Dosage-form class
Divalproex sodium delayed-release tablets: 125, 250 or 500 mg valproic acid activity per tablet; swallow whole without crushing or chewing; not a DEPAKOTE ER extended-release tablet or DEPAKOTE Sprinkle delayed-release capsule
Route
Oral (higher-risk delayed-release tablet exact-product identity field)
Record reviewed
2026-08-29

Copy from the pack in hand

Source-linked reading points

  • The mg figure is strength per tablet, not a daily total, plasma concentration or tablet count. A shared 500 mg label does not permit one-for-one self-substitution between DEPAKOTE delayed-release and DEPAKOTE ER extended-release tablets; any formulation or co-medication change requires clinical and valproate-level review.
  • DEPAKOTE delayed-release tablets are unscored and the label says to swallow whole. Do not crush, chew or divide one to make ‘half’. A swallowing difficulty requires review of the exact prescription and dosage form, not an unreviewed switch to Sprinkle, ER or a liquid.
  • The boxed warning includes potentially fatal hepatotoxicity, fetal risk and pancreatitis. Persistent or severe abdominal pain with nausea or vomiting, marked jaundice or unusual fatigue, or altered awareness needs timely medical assessment; the site does not wait for symptoms to resolve.
  • Older adults may be more sensitive to somnolence and may have a higher unbound drug fraction. Excessive sleepiness, reduced food or fluid intake, dehydration, falls, gait or awareness changes require prompt professional review with the complete medicine list; do not stop or sharply reduce treatment yourself.

Reviewed presentation examples — compare every field

  • Equivalent to valproic acid 125 mg per tablet; 100-tablet bottleNDC 0074-7325-13
  • Equivalent to valproic acid 250 mg per tablet; 100-tablet bottleNDC 0074-7326-13
  • Equivalent to valproic acid 500 mg per tablet; 100-tablet bottleNDC 0074-7327-13

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-29
Source record
4 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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