Perampanel

NDC 51672-4209 · Sun Pharmaceutical Industries, Inc.

Generic namePerampanel

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)PERAMPANEL

Strength12 mg/1

Pharmacologic classAMPA Receptor Antagonists [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Noncompetitive AMPA Glutamate Receptor Antagonist [EPC], UGT1A9 Inhibitors [MoA], UGT2B7 Inhibitors [MoA]

DEA scheduleCIII

Marketing categoryANDA

Packages

51672-4209-2 — 3 BLISTER PACK in 1 CARTON (51672-4209-2) / 10 TABLET, FILM COATED in 1 BLISTER PACK

51672-4209-6 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51672-4209-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0480-7063 — Perampanel, 0480-7065 — Perampanel, 0480-7066 — Perampanel, 0480-7067 — Perampanel, 0480-7068 — Perampanel, 51672-4204 — Perampanel, 51672-4205 — Perampanel, 51672-4206 — Perampanel, 51672-4207 — Perampanel, 51672-4208 — Perampanel, 51672-4256 — PERAMPANEL, 62856-272 — perampanel, 62856-274 — perampanel, 62856-276 — perampanel, 62856-278 — perampanel, 62856-280 — perampanel, 62856-282 — perampanel, 62856-290 — perampanel, 69616-272 — perampanel, 69616-274 — perampanel, +13 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.