NDC 51672-4205 – Perampanel
Perampanel 4 mg/1 · Tablet, Film Coated · Oral
Product NDC51672-4205
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
- Perampanel 4 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4205-2 | 3 BLISTER PACK in 1 CARTON (51672-4205-2) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Nov 25, 2025 |
| 51672-4205-6 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51672-4205-6) | Nov 25, 2025 |
Recalls mentioning this NDC
- D-0628-2026 Jul 1, 2026 · Class II
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.
Other Perampanel products
- 72205-226 Perampanel 12 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-225 Perampanel 10 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-224 Perampanel 8 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-223 Perampanel 6 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-222 Perampanel 4 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-221 Perampanel 2 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-071 Perampanel .5 mg/mL · Suspension · Novadoz Pharmaceuticals LLC
- 51672-4208 Perampanel 10 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 51672-4256 Perampanel .5 mg/mL · Suspension · Sun Pharmaceutical Industries, Inc.
- 51672-4209 Perampanel 12 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 51672-4207 Perampanel 8 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 51672-4206 Perampanel 6 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.