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Lamotrigine

NDC 71205-245, Lamotrigine, tablet, from Proficient Rx LP.

Product NDC
71205-245
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090170
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-245 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE100 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
71205-245-307120502453030 TABLET in 1 BOTTLE, PLASTIC (71205-245-30)
71205-245-607120502456060 TABLET in 1 BOTTLE, PLASTIC (71205-245-60)
71205-245-907120502459090 TABLET in 1 BOTTLE, PLASTIC (71205-245-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/52273d60-3f27-4846-bf40-014ebcf09417

Use it

Look up 71205-245 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-245 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-245. 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.