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Divalproex Sodium

NDC 57237-106, Divalproex Sodium, tablet, delayed release, from Rising Pharma Holdings, Inc..

Product NDC
57237-106
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090554
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57237-106 \
  -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
57237-106-0157237010601100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-01)
57237-106-0557237010605500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6316061c-9758-4f38-9cb2-7ca833dd20bf

  • NADAC price for package 57237010601

    GET /v1/drugs/nadac/57237010601

  • NADAC price for package 57237010605

    GET /v1/drugs/nadac/57237010605

Use it

Look up 57237-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57237-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57237-106. 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.