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Divalproex Sodium

NDC 0832-7122, Divalproex Sodium, tablet, delayed release, from Upsher-Smith Laboratories, LLC.

Product NDC
0832-7122
Status
Listed
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0832-7122 \
  -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
0832-7122-1100832712211100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/02304a23-4a5f-47bc-9687-4044b43f7a20

  • NADAC price for package 00832712211

    GET /v1/drugs/nadac/00832712211

Use it

Look up 0832-7122 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0832-7122 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0832-7122. 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.