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Lamotrigine

NDC 0115-1529, LAMOTRIGINE, tablet, orally disintegrating, from Amneal Pharmaceuticals of New York LLC.

Product NDC
0115-1529
Status
Listed
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200828
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0115-1529 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE200 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
0115-1529-08001151529083 BLISTER PACK in 1 CARTON (0115-1529-08) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0115-1529-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/380bddae-5b31-4965-96de-97711d859d11

Use it

Look up 0115-1529 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0115-1529 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0115-1529. 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.