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Lamotrigine

NDC 71335-1469, Lamotrigine, tablet, film coated, extended release, from Bryant Ranch Prepack.

Product NDC
71335-1469
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200672
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1469 \
  -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
71335-1469-17133514690130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1469-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/36f383af-8b71-4875-85ef-3a7a8b1d8805

Use it

Look up 71335-1469 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1469 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-1469. 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.