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divalproex sodium

NDC 81469-492, divalproex sodium, capsule, coated pellets, from First Nation Group, LLC.

Product NDC
81469-492
Status
Listed
Labeler
First Nation Group, LLC
Dosage form
CAPSULE, COATED PELLETS
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217358
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81469-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM125 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]

Package NDCNDC-11Package
81469-492-0181469049201100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01)
81469-492-10814690492101000 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a76f9909-28c9-4eb7-8ffd-ff6222fea079

Use it

Look up 81469-492 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81469-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81469-492. 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.