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Lamotrigine

NDC 70771-1518, Lamotirigine, tablet, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1518
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207763
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1518 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE250 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
70771-1518-37077115180330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1518-3)
70771-1518-47077115180410 BLISTER PACK in 1 CARTON (70771-1518-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70771-1518-2)
70771-1518-570771151805500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1518-5)
70771-1518-97077115180990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1518-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ecb7a528-699f-4e51-9887-dee60456da2f

Use it

Look up 70771-1518 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1518 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1518. 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.