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LAMOTRIGINE

NDC 69102-639, LAMOTRIGINE, tablet, from OWP Pharmaceuticals, Inc..

Product NDC
69102-639
Status
Listed
Labeler
OWP Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078947
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69102-639 \
  -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
69102-639-096910206390935 TABLET in 1 DOSE PACK (69102-639-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/474fb321-575c-4b97-9dbe-080061652ee4

Use it

Look up 69102-639 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69102-639 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69102-639. 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.