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divalproex sodium

NDC 67046-1631, divalproex sodium, tablet, film coated, extended release, from Coupler LLC.

Product NDC
67046-1631
Status
Listed
Labeler
Coupler LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214643
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1631 \
  -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
67046-1631-36704616310330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1631-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/46b2e8a9-5d50-d0b2-e063-6294a90a1b47

Use it

Look up 67046-1631 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1631 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1631. 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.