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divalproex sodium

NDC 55111-531, divalproex sodium, tablet, delayed release, from Dr.Reddy's Laboratories Limited.

Product NDC
55111-531
Status
Listed
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078755
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-531 \
  -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
55111-531-0155111053101100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01)
55111-531-0555111053105500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05)
55111-531-305511105313030 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30)
55111-531-785511105317810 BLISTER PACK in 1 CARTON (55111-531-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/15f8a5be-e269-2e07-60d9-1dd7bf5f5281

Use it

Look up 55111-531 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-531 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-531. 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.