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Divalproex Sodium

NDC 68084-782, Divalproex Sodium, tablet, delayed release, from American Health Packaging.

Product NDC
68084-782
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090554
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68084-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM500 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]

Package NDCNDC-11Package

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/64b509bc-f398-48ad-bdcb-9904e61d9225

Use it

Look up 68084-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68084-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68084-782. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.