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Lamotrigine

NDC 68382-007, Lamotrigine, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-007
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
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/68382-007 \
  -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
68382-007-0168382000701100 TABLET in 1 BOTTLE (68382-007-01)
68382-007-0568382000705500 TABLET in 1 BOTTLE (68382-007-05)
68382-007-10683820007101000 TABLET in 1 BOTTLE (68382-007-10)
68382-007-166838200071690 TABLET in 1 BOTTLE (68382-007-16)

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 68382-007 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-007 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-007. 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.