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
- 43598-697_108f12cf-4bfc-4406-1d50-d57e656f6c8c
- Product NDC
- 43598-697
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Vigabatrin
- Labeler
- Dr. Reddys Laboratories Inc.,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181121
- Source listing expiry
- 20261231
Source-listed ingredients
- VIGABATRIN — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 PACKET in 1 CARTON (43598-697-50) / 10 mL in 1 PACKET (43598-697-11) · 43598-697-50
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →