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Lamotrigine

NDC 67877-166, Lamotrigine, tablet, from Ascend Laboratories, LLC.

Product NDC
67877-166
Status
Listed
Labeler
Ascend Laboratories, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200694
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67877-166 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE150 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
67877-166-606787701666060 TABLET in 1 BOTTLE (67877-166-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/70cd448a-2921-4c69-bdf2-5a6ce883bd07

Use it

Look up 67877-166 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-166 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-166. 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.