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Vigabatrin

NDC 59651-366, Vigabatrin, powder, for solution, from Aurobindo Pharma Limited.

Product NDC
59651-366
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213899
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-366 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VIGABATRIN500 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]

Package NDCNDC-11Package
59651-366-505965103665050 PACKET in 1 CARTON (59651-366-50) / 1 POWDER, FOR SOLUTION in 1 PACKET (59651-366-07)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c97ce40c-1c5a-479d-9188-5ce03cf7e065

Use it

Look up 59651-366 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-366 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-366. 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.