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Lamotrigine

NDC 65841-682, Lamotrigine, tablet, from Zydus Lifesciences Limited.

Product NDC
65841-682
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077633
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-682 \
  -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
65841-682-0165841068201100 TABLET in 1 BOTTLE (65841-682-01)
65841-682-0565841068205500 TABLET in 1 BOTTLE (65841-682-05)
65841-682-10658410682101000 TABLET in 1 BOTTLE (65841-682-10)
65841-682-116584106821125 TABLET in 1 BOTTLE (65841-682-11)
65841-682-166584106821690 TABLET in 1 BOTTLE (65841-682-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f2f7421-56d4-45d0-9d2d-dc1edaede039

Use it

Look up 65841-682 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-682 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-682. 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.