NDC 51672-4206 – Perampanel

Perampanel 6 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIII 1 recall

Product NDC51672-4206

Product details

Brand name
Perampanel
Generic name
Perampanel
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209538
Marketed since
November 25, 2025
Listing expires
December 31, 2026
Pharmacologic class
Noncompetitive AMPA Glutamate Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Perampanel →

Package NDC codes (2)

Package NDCDescriptionSince
51672-4206-23 BLISTER PACK in 1 CARTON (51672-4206-2) / 10 TABLET, FILM COATED in 1 BLISTER PACKNov 25, 2025
51672-4206-630 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51672-4206-6)Nov 25, 2025

Recalls mentioning this NDC

Other Perampanel products