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divalproex sodium

NDC 60687-904, divalproex sodium, tablet, film coated, extended release, from American Health Packaging.

Product NDC
60687-904
Status
Listed
Labeler
American Health Packaging
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/60687-904 \
  -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
60687-904-0160687090401100 BLISTER PACK in 1 CARTON (60687-904-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-904-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b12b76a0-4b6e-4cd4-9508-10a2c84d8beb

  • NADAC price for package 60687090401

    GET /v1/drugs/nadac/60687090401

Use it

Look up 60687-904 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-904 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-904. 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.