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Lamotrigine

NDC 70518-1153, Lamotrigine, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-1153
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203370
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1153 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE50 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
70518-1153-17051811530150 POUCH in 1 BOX (70518-1153-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-1153-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/de7f61ca-e3c0-4a09-b664-0df2de6a0c30

Use it

Look up 70518-1153 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1153 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1153. 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.