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LAMOTRIGINE

NDC 51672-4252, lamotrigine, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4252
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219677
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4252 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE25 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
51672-4252-65167242520630 TABLET in 1 BOTTLE (51672-4252-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/83297e2e-9199-4b3d-9f44-a921787758fe

  • NADAC price for package 51672425206

    GET /v1/drugs/nadac/51672425206

Use it

Look up 51672-4252 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4252 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4252. 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.