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Lamotrigine

NDC 70518-1908, Lamotrigine, tablet, from REMEDYREPACK INC..

Product NDC
70518-1908
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/70518-1908 \
  -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
70518-1908-17051819080130 TABLET in 1 BLISTER PACK (70518-1908-1)
70518-1908-47051819080430 TABLET in 1 BOTTLE, PLASTIC (70518-1908-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b5646a9-4724-44b8-8cd0-9c14f5e87f86

Use it

Look up 70518-1908 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1908 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1908. 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.