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Lamotrigine

NDC 65862-229, Lamotrigine, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-229
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078956
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-229 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE150 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Dihydrofolate Reductase Inhibitors [MoA]; Mood Stabilizer [EPC]; Organic Cation Transporter 2 Inhibitors [MoA]

Package NDCNDC-11Package
65862-229-0165862022901100 TABLET in 1 BOTTLE (65862-229-01)
65862-229-606586202296060 TABLET in 1 BOTTLE (65862-229-60)
65862-229-786586202297810 BLISTER PACK in 1 CARTON (65862-229-78) / 10 TABLET in 1 BLISTER PACK (65862-229-10)
65862-229-99658620229991000 TABLET in 1 BOTTLE (65862-229-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a9a4309e-fe43-4a26-a30f-c6577d650336

  • NADAC price for package 65862022901

    GET /v1/drugs/nadac/65862022901

  • NADAC price for package 65862022960

    GET /v1/drugs/nadac/65862022960

Use it

Look up 65862-229 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-229 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-229. 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.