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Lamotrigine

NDC 70518-2406, Lamotrigine, tablet, from REMEDYREPACK INC..

Product NDC
70518-2406
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090170
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2406 \
  -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
70518-2406-47051824060430 TABLET in 1 BOTTLE, PLASTIC (70518-2406-4)
70518-2406-57051824060590 TABLET in 1 BOTTLE, PLASTIC (70518-2406-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/346f8af3-b850-48e4-bd6e-82ecafca86d2

Use it

Look up 70518-2406 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2406 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2406. 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.