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LAMICTAL

NDC 0173-0642, lamotrigine, tablet, from GlaxoSmithKline LLC.

Product NDC
0173-0642
Status
Listed
Labeler
GlaxoSmithKline LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020241
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0642 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE100 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
0173-0642-5500173064255100 TABLET in 1 BOTTLE (0173-0642-55)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d7e3572d-56fe-4727-2bb4-013ccca22678

  • NADAC price for package 00173064255

    GET /v1/drugs/nadac/00173064255

Use it

Look up 0173-0642 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0173-0642 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0173-0642. 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.