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lamotrigine

NDC 31722-245, lamotrigine extended-release, tablet, film coated, extended release, from Camber Pharmaceuticals Inc.

Product NDC
31722-245
Status
Listed
Labeler
Camber Pharmaceuticals Inc
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213949
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-245 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LAMOTRIGINE300 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
31722-245-303172202453030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-245-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e45bd69f-3580-ff15-e053-2a95a90a4615

  • NADAC price for package 31722024530

    GET /v1/drugs/nadac/31722024530

Use it

Look up 31722-245 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-245 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-245. 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.