NDC Package 69616-290-38 Fycompa

Perampanel Suspension Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69616-290-38
Package Description:
340 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Fycompa
Non-Proprietary Name:
Perampanel
Substance Name:
Perampanel
Usage Information:
Perampanel is used to treat certain types of seizures (including focal and generalized tonic-clonic seizures). Perampanel belongs to a class of drugs known as anticonvulsants.
11-Digit NDC Billing Format:
69616029038
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
340 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 1356557 - perampanel 2 MG Oral Tablet
  • RxCUI: 1356563 - Fycompa 2 MG Oral Tablet
  • RxCUI: 1356563 - perampanel 2 MG Oral Tablet [FYCOMPA]
  • RxCUI: 1356570 - perampanel 4 MG Oral Tablet
  • RxCUI: 1356572 - Fycompa 4 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Catalyst Pharmaceuticals, Inc.
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA208277
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-02-2024
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69616-290-38?

    The NDC Packaged Code 69616-290-38 is assigned to a package of 340 ml in 1 bottle of Fycompa, a human prescription drug labeled by Catalyst Pharmaceuticals, Inc.. The product's dosage form is suspension and is administered via oral form.

    Is NDC 69616-290 included in the NDC Directory?

    Yes, Fycompa with product code 69616-290 is active and included in the NDC Directory. The product was first marketed by Catalyst Pharmaceuticals, Inc. on January 02, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 69616-290-38?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 340.

    What is the 11-digit format for NDC 69616-290-38?

    The 11-digit format is 69616029038. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-269616-290-385-4-269616-0290-38