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Felbatol

NDC 0037-0431, felbamate, tablet, from Viatris Specialty LLC.

Product NDC
0037-0431
Status
Listed
Labeler
Viatris Specialty LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020189
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0037-0431 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FELBAMATE600 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
0037-0431-0100037043101100 TABLET in 1 BOTTLE, PLASTIC (0037-0431-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2f522701-397a-11de-8a39-0800200c9a66

  • NADAC price for package 00037043101

    GET /v1/drugs/nadac/00037043101

Use it

Look up 0037-0431 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0037-0431 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0037-0431. 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.