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vigabatrin

NDC 70710-1287, vigabatrin, tablet, film coated, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
70710-1287
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215707
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1287 \
  -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
70710-1287-170710128701100 TABLET, FILM COATED in 1 BOTTLE (70710-1287-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6c0bf4fb-b234-4053-9163-1e8d0142d718

Use it

Look up 70710-1287 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1287 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1287. 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.