NDC 59651-367 – Vigabatrin

Vigabatrin 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59651-367

Product details

Brand name
Vigabatrin
Generic name
Vigabatrin
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215601
Marketed since
May 10, 2022
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Vigabatrin →

Package NDC codes (1)

Package NDCDescriptionSince
59651-367-011 BOTTLE in 1 CARTON (59651-367-01) / 100 TABLET in 1 BOTTLEMay 10, 2022

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