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divalproex sodium

NDC 0615-8586, divalproex sodium, tablet, delayed release, from NCS HealthCare of KY, LLC dba Vangard Labs.

Product NDC
0615-8586
Status
Listed
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
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/0615-8586 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM125 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0615-8586-390061585863930 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8586-39)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f936b9d0-a58f-4fa5-8db9-752dabb837a6

Use it

Look up 0615-8586 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8586 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0615-8586. 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.