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divalproex sodium

NDC 69452-435, divalproex sodium, tablet, delayed release, from Bionpharma Inc..

Product NDC
69452-435
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078853
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-435 \
  -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
69452-435-136945204351330 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-13)
69452-435-2069452043520100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20)
69452-435-3069452043530500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/19064624-81d1-4ce3-bfe4-955bad6af6a2

  • NADAC price for package 69452043520

    GET /v1/drugs/nadac/69452043520

  • NADAC price for package 69452043530

    GET /v1/drugs/nadac/69452043530

Use it

Look up 69452-435 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-435 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-435. 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.