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  5. NDC Package Code: 81968-351-07 Sunosi

NDC Package 81968-351-07 Sunosi

Solriamfetol Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
81968-351-07
Package Description:
7 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
81968-351
Proprietary Name:
Sunosi
Non-Proprietary Name:
Solriamfetol
Substance Name:
Solriamfetol
Usage Information:
This medication is used to improve wakefulness in people that have too much daytime sleepiness due to certain sleep problems (narcolepsy, obstructive sleep apnea). It may work by changing the amounts of certain substances (dopamine, norepinephrine) in your body. This medication is not used to treat the cause of obstructive sleep apnea-OSA. Continue treatment for OSA, such as using continuous positive airway pressure (CPAP), while using this medication.
11-Digit NDC Billing Format:
81968035107
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
7 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2121756 - solriamfetol 75 MG Oral Tablet
  • RxCUI: 2121756 - solriamfetol 75 MG (equivalent to solriamfetol HCl 89.3 MG) Oral Tablet
  • RxCUI: 2121758 - solriamfetol 150 MG Oral Tablet
  • RxCUI: 2121758 - solriamfetol 150 MG (equivalent to solriamfetol HCl 178.5 MG) Oral Tablet
  • RxCUI: 2121764 - sunosi 75 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Axsome Therapeutics, Inc.
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SOLRIAMFETOL 150 mg/1
    • DEA Schedule:
    Schedule IV (CIV) Substances
    Sample Package:
    Yes
    FDA Application Number:
    NDA211230
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-18-2019
    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
    81968-351-0130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
    81968-351-1010 BLISTER PACK in 1 CARTON / 7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 81968-351-07?

    The NDC Packaged Code 81968-351-07 is assigned to a package of 7 tablet, film coated in 1 blister pack of Sunosi, a human prescription drug labeled by Axsome Therapeutics, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 81968-351 included in the NDC Directory?

    Yes, Sunosi with product code 81968-351 is active and included in the NDC Directory. The product was first marketed by Axsome Therapeutics, Inc. on June 18, 2019 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 81968-351-07?

    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 7.

    What is the 11-digit format for NDC 81968-351-07?

    The 11-digit format is 81968035107. 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
    5-3-281968-351-075-4-281968-0351-07