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  5. NDC Package Code: 76204-010-55 Albuterol Sulfate Inhalation Solution

NDC Package 76204-010-55 Albuterol Sulfate Inhalation Solution

Albuterol Sulfate Solution Respiratory (inhalation) - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. 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:
76204-010-55
Package Description:
25 POUCH in 1 CARTON / 5 VIAL in 1 POUCH (76204-010-05) / 3 mL in 1 VIAL
Product Code:
76204-010
Proprietary Name:
Albuterol Sulfate Inhalation Solution
Non-Proprietary Name:
Albuterol Sulfate
Substance Name:
Albuterol Sulfate
Usage Information:
Albuterol (also known as salbutamol) is used to treat wheezing and shortness of breath caused by breathing problems such as asthma. It is a quick-relief medication. Albuterol belongs to a class of drugs known as bronchodilators. It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Controlling symptoms of breathing problems can decrease time lost from work or school.
11-Digit NDC Billing Format:
76204001055
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 351136 - albuterol sulfate 0.042 % (1.25 MG/3 ML) Inhalation Solution
  • RxCUI: 351136 - albuterol 0.417 MG/ML Inhalation Solution
  • RxCUI: 351136 - albuterol 0.042 % (1.25 MG/3 ML) Inhalation Solution
  • RxCUI: 351136 - albuterol 1.25 MG (albuterol sulfate 1.5 MG) per 3 ML Inhalation Solution
  • RxCUI: 351137 - albuterol sulfate 0.021 % (0.63 MG/3 ML) Inhalation Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ritedose Pharmaceuticals, Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
    • Active Ingredient(s):
  • ALBUTEROL SULFATE .63 mg/3mL
    • Pharmacologic Class(es):
  • Adrenergic beta2-Agonists - [MoA] (Mechanism of Action)
  • beta2-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA214531
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-04-2022
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 76204-010-55 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    76204001055J7613Albuterol non-comp unit1 MG3250.6315.75

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    76204-010-0130 POUCH in 1 CARTON / 1 VIAL in 1 POUCH (76204-010-11) / 3 mL in 1 VIAL

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 76204-010-55?

    The NDC Packaged Code 76204-010-55 is assigned to a package of 25 pouch in 1 carton / 5 vial in 1 pouch (76204-010-05) / 3 ml in 1 vial of Albuterol Sulfate Inhalation Solution, a human prescription drug labeled by Ritedose Pharmaceuticals, Llc. The product's dosage form is solution and is administered via respiratory (inhalation) form.

    Is NDC 76204-010 included in the NDC Directory?

    Yes, Albuterol Sulfate Inhalation Solution with product code 76204-010 is active and included in the NDC Directory. The product was first marketed by Ritedose Pharmaceuticals, Llc on January 04, 2022 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 76204-010-55?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 76204-010-55?

    The 11-digit format is 76204001055. 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
    5-3-276204-010-555-4-276204-0010-55