NDC 70771-1654 – Vigabatrin

Vigabatrin 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1654

Product details

Brand name
Vigabatrin
Generic name
Vigabatrin
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215707
Marketed since
January 20, 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
70771-1654-1100 TABLET, FILM COATED in 1 BOTTLE (70771-1654-1)Jan 20, 2022

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