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Lamotrigine

NDC 51672-4130, Lamotrigine, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4130
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078525
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4130 \
  -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
51672-4130-05167241300010 BLISTER PACK in 1 CARTON (51672-4130-0) / 10 TABLET in 1 BLISTER PACK
51672-4130-151672413001100 TABLET in 1 BOTTLE (51672-4130-1)
51672-4130-3516724130031000 TABLET in 1 BOTTLE (51672-4130-3)
51672-4130-45167241300460 TABLET in 1 BOTTLE (51672-4130-4)
51672-4130-65167241300630 TABLET in 1 BOTTLE (51672-4130-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b829f9b2-f0ac-408a-a6f4-18b72150227d

  • NADAC price for package 51672413001

    GET /v1/drugs/nadac/51672413001

Use it

Look up 51672-4130 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4130 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4130. 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.