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    Ipratropium Bromide

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    Phenoterol Hydrobromide; Ipratropium Bromide

    Brand Name : Ipratropiumbromid+Fenoterolhydrobromid \"Farmak\"

    Dosage Form : Solution For Inhalation

    Dosage Strength : 0.5mg/4ml; 1.25mg/4ml

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    Approval Date : 14-03-2025

    Application Number : 28107059023

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    Ipratropium Bromide (Monohydrate); Salbutamol Sulfate

    Brand Name : Ipratropium/Salbutamol Orion

    Dosage Form : Inhalation Solution

    Dosage Strength : 0.5mg/2.5ml;2.5mg/2.5ml

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    Approval Date : 06/11/2014

    Application Number : 20130808000088

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    Xylometazoline; Ipratropium Bromide

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    Dosage Form : Nasal Spray

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    Ipratropium Bromide; Salbutamol Sulfate

    Brand Name : Ipratropium/Salbutamol \"Orion\"

    Dosage Form : Nebulizer Inhalation Solution

    Dosage Strength : 0.5mg/inh; 2.5mg/inh

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    Approval Date : 13-11-2014

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    Phenoterol Hydrobromide; Ipratropium Bromide

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    Approval Date : 1986-12-29

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    Brand Name : ATROVENT

    Dosage Form : SOLUTION;INHALATION

    Dosage Strength : 0.02% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1993-09-29

    Application Number : 20228

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    ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

    Brand Name : COMBIVENT

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : EQ 0.09MG BASE/INH;0.018MG/INH

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    Approval Date : 1996-10-24

    Application Number : 20291

    Regulatory Info : DISCN

    Registration Country : USA

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    Boehringer Ingelheim GmbH

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    IPRATROPIUM BROMIDE

    Brand Name : ATROVENT

    Dosage Form : SPRAY, METERED;NASAL

    Dosage Strength : 0.021MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1995-10-20

    Application Number : 20393

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    Boehringer Ingelheim GmbH

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    IPRATROPIUM BROMIDE

    Brand Name : ATROVENT

    Dosage Form : SPRAY, METERED;NASAL

    Dosage Strength : 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1995-10-20

    Application Number : 20394

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    IPRATROPIUM BROMIDE

    Brand Name : ATROVENT HFA

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : 0.021MG/INH

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    Approval Date : 2004-11-27

    Application Number : 21527

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    ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

    Brand Name : COMBIVENT RESPIMAT

    Dosage Form : SPRAY, METERED;INHALATION

    Dosage Strength : EQ 0.1MG BASE/INH;0.02MG/INH

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    Approval Date : 2011-10-07

    Application Number : 21747

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    Phenoterol Hydrobromide; Ipratropium Bromide

    Brand Name : Berodual

    Dosage Form : Nebulizer Inhalation Solution

    Dosage Strength : 1.25mg/inh; 0.5mg/inh

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    Approval Date : 04-02-1993

    Application Number : 28101497592

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    Phenoterol Hydrobromide; Ipratropium Bromide

    Brand Name : Berodual

    Dosage Form : Inhalation Spray

    Dosage Strength : 50mcg/inh; 20mcg/inh

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    Approval Date : 14-02-2001

    Application Number : 28103223300

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    Ipratropium Bromide Monohydrate

    Brand Name : Atrovent

    Dosage Form : Nebulizer Inhalation Solution

    Dosage Strength : 0.25mg/ml

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    Approval Date : 03-06-1986

    Application Number : 28101230985

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    ORIFARM GROUP AS

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    Phenoterol Hydrobromide; Ipratropium Bromide

    Brand Name : Duovent

    Dosage Form : Nebulizer Inhalation Solution

    Dosage Strength : 1.25mg/inh; 0.5mg/inh

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    Approval Date : 06-03-2002

    Application Number : 28103266201

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    Brand Name : Duovent

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    Dosage Strength : 1.25mg/inh; 0.5mg/inh

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    Approval Date : 05-07-2023

    Application Number : 28106978123

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    Teva Pharmaceutical Industries

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    Ipratropium Bromide; Salbutamol Sulfate

    Brand Name : Ipramol Steri-Neb

    Dosage Form : Nebulizer Inhalation Solution

    Dosage Strength : 2.5mg/inh; 0.5 mg/inh

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    Approval Date : 12-12-2007

    Application Number : 28104130807

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    ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

    Brand Name : DUONEB

    Dosage Form : SOLUTION;INHALATION

    Dosage Strength : EQ 0.083% BASE;0.017% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2001-03-21

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