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  5. NDC Package Code: 47335-703-52 Albuterol Sulfate

NDC Package 47335-703-52 Albuterol Sulfate

Solution Respiratory (inhalation) - 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:
47335-703-52
Package Description:
6 POUCH in 1 CARTON / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL
Product Code:
47335-703
Proprietary Name:
Albuterol Sulfate
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:
47335070352
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 630208 - albuterol sulfate 0.083 % Inhalation Solution
  • RxCUI: 630208 - albuterol 0.83 MG/ML Inhalation Solution
  • RxCUI: 630208 - albuterol 0.083 % Inhalation Solution
  • RxCUI: 630208 - albuterol 0.83 MG/ML (albuterol sulfate 1 MG/ML) Inhalation Solution
  • RxCUI: 630208 - albuterol 2.5 MG per 3 ML Inhalation Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sun Pharmaceutical Industries, Inc.
    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 .83 mg/mL
    • Pharmacologic Class(es):
  • Adrenergic beta2-Agonists - [MoA] (Mechanism of Action)
  • beta2-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA207857
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-11-2021
    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
    47335-703-495 POUCH in 1 CARTON / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL
    47335-703-5412 POUCH in 1 CARTON / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 47335-703-52?

    The NDC Packaged Code 47335-703-52 is assigned to a package of 6 pouch in 1 carton / 5 vial in 1 pouch / 3 ml in 1 vial of Albuterol Sulfate, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is solution and is administered via respiratory (inhalation) form.

    Is NDC 47335-703 included in the NDC Directory?

    Yes, Albuterol Sulfate with product code 47335-703 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on June 11, 2021 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 47335-703-52?

    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 47335-703-52?

    The 11-digit format is 47335070352. 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
    5-3-247335-703-525-4-247335-0703-52