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Divalproex Sodium

NDC 55111-534, Divalproex Sodium, tablet, film coated, extended release, from Dr. Reddy's Laboratories Ltd.

Product NDC
55111-534
Status
Listed
Labeler
Dr. Reddy's Laboratories Ltd
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090070
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-534 \
  -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
55111-534-0155111053401100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-01)
55111-534-0555111053405500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-05)
55111-534-305511105343030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-30)
55111-534-605511105346060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fa823ee0-0c69-6b85-da1e-9bb2e2150ea5

  • NADAC price for package 55111053401

    GET /v1/drugs/nadac/55111053401

  • NADAC price for package 55111053405

    GET /v1/drugs/nadac/55111053405

Use it

Look up 55111-534 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-534 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-534. 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.