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Divalproex sodium

NDC 31722-021, Divalproex sodium, tablet, film coated, extended release, from Camber Pharmaceuticals, Inc..

Product NDC
31722-021
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215527
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-021 \
  -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
31722-021-0131722002101100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-01)
31722-021-0531722002105500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e8e954d4-54e3-491c-867c-b3b656b70f23

  • NADAC price for package 31722002101

    GET /v1/drugs/nadac/31722002101

  • NADAC price for package 31722002105

    GET /v1/drugs/nadac/31722002105

Use it

Look up 31722-021 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-021 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-021. 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.