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  5. NDC Package Code: 69097-840-64 Ipratropium Bromide And Albuterol Sulfate

NDC Package 69097-840-64 Ipratropium Bromide And 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:
69097-840-64
Package Description:
2 POUCH in 1 CARTON / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL
Product Code:
69097-840
Proprietary Name:
Ipratropium Bromide And Albuterol Sulfate
Non-Proprietary Name:
Ipratropium Bromide And Albuterol Sulfate
Substance Name:
Albuterol Sulfate; Ipratropium Bromide
Usage Information:
Ipratropium Bromide and Albuterol Sulfate Inhalation Solution is indicated for the treatment of bronchospasm associated with COPD in patients requiring more than one bronchodilator.
11-Digit NDC Billing Format:
69097084064
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1437702 - ipratropium Br 0.5 MG / albuterol sulfate 3 MG in 3 ML Inhalation Solution
  • RxCUI: 1437702 - albuterol 0.833 MG/ML / ipratropium bromide 0.167 MG/ML Inhalation Solution
  • RxCUI: 1437702 - albuterol 2.5 MG (as albuterol sulfate 3 MG) / ipratropium bromide 0.5 MG per 3 ML Inhalation Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cipla Usa 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 2.5 mg/3mL
  • IPRATROPIUM BROMIDE .5 mg/3mL
    • Pharmacologic Class(es):
  • Adrenergic beta2-Agonists - [MoA] (Mechanism of Action)
  • Anticholinergic - [EPC] (Established Pharmacologic Class)
  • Cholinergic Antagonists - [MoA] (Mechanism of Action)
  • beta2-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA202496
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-01-2020
    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.

    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 69097-840-64 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    69097084064J7620Albuterol ipratrop non-comp2.5 MG/0.5 MG360160

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    69097-840-5330 POUCH in 1 CARTON / 1 VIAL in 1 POUCH (69097-840-34) / 3 mL in 1 VIAL
    69097-840-871 POUCH in 1 CARTON / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69097-840-64?

    The NDC Packaged Code 69097-840-64 is assigned to a package of 2 pouch in 1 carton / 30 vial in 1 pouch / 3 ml in 1 vial of Ipratropium Bromide And Albuterol Sulfate, a human prescription drug labeled by Cipla Usa Inc.. The product's dosage form is solution and is administered via respiratory (inhalation) form.

    Is NDC 69097-840 included in the NDC Directory?

    Yes, Ipratropium Bromide And Albuterol Sulfate with product code 69097-840 is active and included in the NDC Directory. The product was first marketed by Cipla Usa Inc. on June 01, 2020 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 69097-840-64?

    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 69097-840-64?

    The 11-digit format is 69097084064. 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
    5-3-269097-840-645-4-269097-0840-64