NDC 70771-1742 – vigabatrin

Vigabatrin 500 mg/10mL · Powder, For Solution · Oral

Human Prescription Drug

Product NDC70771-1742

Product details

Brand name
vigabatrin
Generic name
vigabatrin
Labeler
Zydus Lifesciences Limited
Dosage form
Powder, For Solution
Route
Oral
Marketing category
ANDA · ANDA214671
Marketed since
March 24, 2025
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
70771-1742-850 PACKET in 1 CARTON (70771-1742-8) / 10 mL in 1 PACKET (70771-1742-1)Mar 24, 2025

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