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Vigabatrin

NDC 0591-3851, Vigabatrin, tablet, film coated, from Actavis Pharma, Inc..

Product NDC
0591-3851
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209822
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3851 \
  -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
0591-3851-0100591385101100 TABLET, FILM COATED in 1 BOTTLE (0591-3851-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8dc7bd15-2636-4d58-b651-dd117ca43dbd

Use it

Look up 0591-3851 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3851 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-3851. 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.