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divalproex sodium

NDC 67046-1647, divalproex sodium, tablet, delayed release, from Coupler LLC.

Product NDC
67046-1647
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078853
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1647 \
  -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
67046-1647-36704616470330 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1647-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4834732f-6044-946c-e063-6394a90a5da3

Use it

Look up 67046-1647 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1647 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1647. 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.