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Lacosamide

NDC 47335-943, Lacosamide, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-943
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205031
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-943 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACOSAMIDE150 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
47335-943-18473350943181000 TABLET, FILM COATED in 1 BOTTLE (47335-943-18)
47335-943-8247335094382180 TABLET, FILM COATED in 1 BOTTLE (47335-943-82)
47335-943-864733509438660 TABLET, FILM COATED in 1 BOTTLE (47335-943-86)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2098d3a5-776e-4b52-8ade-80a3ab7b3de7

  • NADAC price for package 47335094386

    GET /v1/drugs/nadac/47335094386

Use it

Look up 47335-943 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-943 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-943. 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.