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Lamotrigine

NDC 69918-370, Lamotrigine, tablet, from Nordic Pharma, Inc..

Product NDC
69918-370
Status
Listed
Labeler
Nordic Pharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214124
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69918-370 \
  -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
69918-370-306991803703030 TABLET in 1 BOTTLE (69918-370-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/67cf961e-02b9-4a99-944f-43a55df6a544

  • NADAC price for package 69918037030

    GET /v1/drugs/nadac/69918037030

Use it

Look up 69918-370 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69918-370 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69918-370. 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.