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Divalproex Sodium D/R

NDC 72189-636, Divalproex Sodium D/R, tablet, delayed release, from Direct_Rx.

Product NDC
72189-636
Status
Listed
Labeler
Direct_Rx
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078597
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-636 \
  -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
72189-636-607218906366060 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3aff8f08-d8e8-cd13-e063-6394a90aa00c

Use it

Look up 72189-636 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-636 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-636. 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.