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Lacosamide

NDC 65862-748, Lacosamide, tablet, film coated, from Aurobindo Pharma Limited.

Product NDC
65862-748
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204994
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-748 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACOSAMIDE100 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
65862-748-03658620748033 BLISTER PACK in 1 CARTON (65862-748-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-748-10)
65862-748-606586207486060 TABLET, FILM COATED in 1 BOTTLE (65862-748-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6140b3f1-ff60-427c-91d7-15af99fd78f1

  • NADAC price for package 65862074860

    GET /v1/drugs/nadac/65862074860

Use it

Look up 65862-748 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-748 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-748. 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.