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Lamotrigine

NDC 50228-322, Lamotrigine, tablet, orally disintegrating, from ScieGen Pharmaceuticals, Inc..

Product NDC
50228-322
Status
Listed
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206382
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50228-322 \
  -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
50228-322-0150228032201100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (50228-322-01)
50228-322-305022803223030 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (50228-322-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/de700ac1-4048-467e-abb1-238953261a97

Use it

Look up 50228-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50228-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50228-322. 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.