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Divalproex Sodium

NDC 60687-868, Divalproex Sodium, tablet, delayed release, from American Health Packaging.

Product NDC
60687-868
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079163
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-868 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
60687-868-0160687086801100 BLISTER PACK in 1 CARTON (60687-868-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-868-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ca6bbec6-5631-4436-957e-fb8707e1683d

  • NADAC price for package 60687086801

    GET /v1/drugs/nadac/60687086801

Use it

Look up 60687-868 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-868 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-868. 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.