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
- 70710-1494_b41c9be1-67c2-416e-ae53-5c31eafb8e10
- Product NDC
- 70710-1494
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- vigabatrin
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250324
- Source listing expiry
- 20261231
Source-listed ingredients
- VIGABATRIN — 500 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 PACKET in 1 CARTON (70710-1494-8) / 10 mL in 1 PACKET (70710-1494-1) · 70710-1494-8
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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