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Lamotrigine ER

NDC 72189-560, Lamotrigine ER, tablet, film coated, extended release, from Direct_rx.

Product NDC
72189-560
Status
Listed
Labeler
Direct_rx
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213949
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-560 \
  -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
72189-560-307218905603030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-560-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b42a7cf-86d8-e506-e063-6394a90a3c9b

Use it

Look up 72189-560 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-560 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-560. 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.