United States · FDA National Drug Code directory
VIGAFYDE
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
- 80789-003_43aeb38a-b4ee-47ed-8239-c488b074f1c9
- Product NDC
- 80789-003
- Form
- SOLUTION
- Composition / generic term
- vigabatrin
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20240618
- Source listing expiry
- 20271231
Source-listed ingredients
- VIGABATRIN — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (80789-003-15) / 150 mL in 1 BOTTLE · 80789-003-15
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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