Prescription drug · ANDA
Perampanel NDC 51672-4209
Perampanel 12 mg/1 · Tablet, Film coated · Oral · Sun Pharmaceutical Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51672-4209-2 | 51672420902 | 3 BLISTER PACK in 1 CARTON (51672-4209-2) / 10 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Nov 25, 2025 | |
| 51672-4209-6 | 51672420906 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51672-4209-6)Marketed from Nov 25, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Perampanel
- Generic name (nonproprietary)
- perampanel
- Active ingredients
- Perampanel — 12 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209538
- Marketing start
- Listing expires
- DEA schedule
- CIII
- Other FDA classes
- AMPA Receptor Antagonists (Mechanism)Cytochrome P450 2C8 Inhibitors (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)UGT1A9 Inhibitors (Mechanism)UGT2B7 Inhibitors (Mechanism)
- Identifiers
- Product ID 51672-4209_4653e298-d84f-dc92-e063-6294a90a2d75SPL ID 4653e298-d84f-dc92-e063-6294a90a2d75SPL set ID 1b0458ea-e718-4d48-ae55-ad9b4d863810RxCUI 1356557, 1356570, 1356574, 1356578, 1356582, 1356586UNII H821664NPKUPC 0351672420567, 0351672420666, 0351672420765, 0351672420963, 0351672420468
- Pharmacologic class
- Noncompetitive AMPA Glutamate Receptor Antagonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N451672420902followed by a unit qualifier and the quantityPackage 51672-4209-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
Perampanel tablets, a non-competitive AMPA glutamate receptor antagonist, is indicated for: Treatment of partial-onset seizures with or without secondarily generalized seizures in patients with epilepsy 4 years of age and older ( 1.1 ) Adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients with epilepsy 12 years of age and older ( 1.2 ) 1.1 Partial-Onset Seizures Perampanel tablets are indicated for the treatment of partial-onset seizures with or without secondarily generalized seizures in patients with epilepsy 4 years of age and older. 1.2 Primary Generalized Tonic-Clonic Seizures Perampanel tablets are indicated as adjunctive therapy for the treatment…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 209538
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Perampanel | Perampanel 6 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4206 |
| Perampanel | Perampanel 2 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4204 |
| Perampanel | Perampanel 4 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4205 |
| Perampanel | Perampanel 8 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4207 |
| Perampanel | Perampanel 10 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 51672-4208 |