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Divalproex Sodium

NDC 48433-034, divalproex sodium, tablet, film coated, extended release, from Safecor Health, LLC.

Product NDC
48433-034
Status
Listed
Labeler
Safecor Health, LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077567
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/48433-034 \
  -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
48433-034-084843300340880 BLISTER PACK in 1 CARTON (48433-034-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (48433-034-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3aec1944-86a1-490c-a734-d9dd3b52c9d6

Use it

Look up 48433-034 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/48433-034 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 48433-034. 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.