NDC Package 13551-001-30 Lumryz

Sodium Oxybate For Suspension, Extended Release 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:
13551-001-30
Package Description:
30 PACKET in 1 CARTON / 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKET
Product Code:
Proprietary Name:
Lumryz
Non-Proprietary Name:
Sodium Oxybate
Substance Name:
Sodium Oxybate
Usage Information:
This medication is used to treat narcolepsy, a condition that causes severe daytime sleepiness. Sodium oxybate can decrease daytime sleepiness and also reduce the number of sudden short attacks of weak/paralyzed muscles (known as cataplexy) that can occur in patients with narcolepsy. Sodium oxybate is a central nervous system depressant. It is also known as gamma hydroxybutyrate (GHB).
11-Digit NDC Billing Format:
13551000130
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2636822 - sodium oxybate 4.5 GM Granules for extended release Oral Suspension
  • RxCUI: 2636822 - sodium oxybate 4500 MG Granules for Oral Suspension
  • RxCUI: 2636822 - sodium oxybate 4.5 GM (equivalent to 3.7 GM oxybate) Granules for Oral Suspension
  • RxCUI: 2636828 - Lumryz 4.5 GM Granules for extended release Oral Suspension
  • RxCUI: 2636828 - sodium oxybate 4500 MG Granules for Oral Suspension [Lumryz]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Avadel Cns Pharmaceuticals, Llc
    Dosage Form:
    For Suspension, Extended Release - A product, usually a solid, intended for suspension prior to administration; once the suspension is administered, the drug will be released at a constant rate over a specified period.
    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:
    NDA214755
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-01-2023
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    13551-001-077 PACKET in 1 CARTON / 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 13551-001-30?

    The NDC Packaged Code 13551-001-30 is assigned to a package of 30 packet in 1 carton / 1 for suspension, extended release in 1 packet of Lumryz, a human prescription drug labeled by Avadel Cns Pharmaceuticals, Llc. The product's dosage form is for suspension, extended release and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

    Is NDC 13551-001 included in the NDC Directory?

    Yes, Lumryz with product code 13551-001 is active and included in the NDC Directory. The product was first marketed by Avadel Cns Pharmaceuticals, Llc on May 01, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 13551-001-30?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

    What is the 11-digit format for NDC 13551-001-30?

    The 11-digit format is 13551000130. 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
    5-3-213551-001-305-4-213551-0001-30