Skip to content
healthcare.dev

DIVALPROEX SODIUM

NDC 61919-249, divalproex sodium, tablet, delayed release, from DirectRx.

Product NDC
61919-249
Status
Listed
Labeler
DirectRx
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/61919-249 \
  -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
61919-249-306191902493030 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-30)
61919-249-606191902496060 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce12c7b1-caa9-4224-bb5f-3e20e0281d66

Use it

Look up 61919-249 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61919-249 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61919-249. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.