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Lamotrigine

NDC 68382-108, Lamotrigine, tablet, chewable, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-108
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, CHEWABLE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078009
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE5 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
68382-108-0168382010801100 TABLET, CHEWABLE in 1 BOTTLE (68382-108-01)
68382-108-0568382010805500 TABLET, CHEWABLE in 1 BOTTLE (68382-108-05)
68382-108-166838201081690 TABLET, CHEWABLE in 1 BOTTLE (68382-108-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e849033b-a3bc-408e-88de-7cd1d2660949

Use it

Look up 68382-108 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-108. 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.