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Divalproex Sodium

NDC 68001-106, Divalproex Sodium, tablet, film coated, extended release, from BluePoint Laboratories.

Product NDC
68001-106
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078239
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-106 \
  -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
68001-106-0068001010600100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-00)
68001-106-0368001010603500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b12c694-e120-45f6-ad28-36373e2c5378

  • NADAC price for package 68001010600

    GET /v1/drugs/nadac/68001010600

  • NADAC price for package 68001010603

    GET /v1/drugs/nadac/68001010603

Use it

Look up 68001-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-106. 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.