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Divalproex Sodium

NDC 68001-472, Divalproex Sodium, tablet, delayed release, from BluePoint Laboratories.

Product NDC
68001-472
Status
Listed
Labeler
BluePoint Laboratories
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/68001-472 \
  -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
68001-472-0068001047200100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00)
68001-472-0368001047203500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b95494e2-ee7a-7415-e053-2995a90ae852

  • NADAC price for package 68001047200

    GET /v1/drugs/nadac/68001047200

  • NADAC price for package 68001047203

    GET /v1/drugs/nadac/68001047203

Use it

Look up 68001-472 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-472 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-472. 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.