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Lamotrigine

NDC 68071-3514, Lamotrigine, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3514
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077633
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3514 \
  -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
68071-3514-66807135140660 TABLET in 1 BOTTLE (68071-3514-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/065e97c9-3c5f-16e6-e063-6294a90a13fc

Use it

Look up 68071-3514 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3514 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3514. 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.