United States · FDA National Drug Code directory
vigabatrin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 80005-167_533a7f8e-4ac6-4688-9ea0-a90626c86ab8
- Product NDC
- 80005-167
- Form
- TABLET, FILM COATED
- Composition / generic term
- vigabatrin
- Labeler
- Carnegie Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260218
- Source listing expiry
- 20271231
Source-listed ingredients
- VIGABATRIN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (80005-167-11) / 100 TABLET, FILM COATED in 1 BOTTLE · 80005-167-11
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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