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Divalproex Sodium

NDC 87441-028, Divalproex Sodium, tablet, delayed release, from Unit Dose Solutions, Inc..

Product NDC
87441-028
Status
Listed
Labeler
Unit Dose Solutions, Inc.
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/87441-028 \
  -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
87441-028-018744100280130 TABLET, DELAYED RELEASE in 1 BLISTER PACK (87441-028-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/547d8305-bfc5-f4da-e063-6294a90a6106

Use it

Look up 87441-028 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87441-028 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87441-028. 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.