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    Bayer AG

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    Regulatory Info : RX

    Registration Country : USA

    CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 250MG BASE

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    Approval Date : 1987-10-22

    Application Number : 19537

    Regulatory Info : RX

    Registration Country : USA

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    Aspen Pharmacare Holdings

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    Regulatory Info : Generic

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    Ciprofloxacin Hydrochloride Monohydrate

    Brand Name : Otixal

    Dosage Form : EAR

    Dosage Strength : 3mg

    Packaging : 10X1mg

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    Orion Corporation

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    Ciprofloxacin Hydrochloride Monohydrate

    Brand Name : Ciprofloxacin \"Orion\"

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250mg

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    Approval Date : 21-11-2016

    Application Number : 28105813416

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    Towa International

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    Regulatory Info : Suspended

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    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Think

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250MG

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    Approval Date : 21-03-2000

    Application Number : 62962

    Regulatory Info : Suspended

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    Hebei AiYoung Pharmaceutical Techno...

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    Virtual BoothHebei AiYoung Pharmaceutical Technology delivering high-quality APIs, intermediates, and end-to-end pharma solutions globally.

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    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Hydrochloride

    Dosage Form : Injection

    Dosage Strength : 0.2G

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    Bayer AG

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    Regulatory Info : RX

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    CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 500MG BASE

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    Approval Date : 1987-10-22

    Application Number : 19537

    Regulatory Info : RX

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    Regulatory Info : DISCN

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    CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 750MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1987-10-22

    Application Number : 19537

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Bayer AG

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    Regulatory Info : DISCN

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    CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO XR

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 212.6MG;EQ 287.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2002-12-13

    Application Number : 21473

    Regulatory Info : DISCN

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    09

    Bayer AG

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    Regulatory Info : DISCN

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    CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO XR

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 425.2MG;EQ 574.9MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2003-08-28

    Application Number : 21473

    Regulatory Info : DISCN

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    Regulatory Info :

    Registration Country : USA

    CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO XR

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Dosage Strength : 212.6MG; EQ 287.5MG BASE

    Packaging :

    Approval Date :

    Application Number : 21554

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    Registration Country : USA

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    11

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    CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO XR

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Dosage Strength : 425.2MG; EQ 574.9MG BASE

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    Application Number : 21554

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    Regulatory Info : Cancelled

    Registration Country : Spain

    Ciprofloxacin Hydrochloride

    Brand Name : Baycip Otico

    Dosage Form : Ear Drop In Solution In Single-Dose Containers

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 01-12-1997

    Application Number : 61558

    Regulatory Info : Cancelled

    Registration Country : Spain

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    Regulatory Info : Cancelled

    Registration Country : Spain

    Ciprofloxacin Hydrochloride

    Brand Name : Baycip

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 01-05-1988

    Application Number : 57973

    Regulatory Info : Cancelled

    Registration Country : Spain

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    Bayer AG

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Ciproxin

    Dosage Form : Tablet

    Dosage Strength : 250mg

    Packaging :

    Approval Date : 05-02-1988

    Application Number : 1.99E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Bayer AG

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    Regulatory Info : Deregistered

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    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Ciproxin

    Dosage Form : Tablet

    Dosage Strength : 750mg

    Packaging :

    Approval Date : 05-02-1988

    Application Number : 1.99E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Regulatory Info : Deregistered

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    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Ciproxin

    Dosage Form : Tablet

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 08-09-1989

    Application Number : 1.99E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Regulatory Info : Deregistered

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    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Baycip

    Dosage Form : Tablet

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 11-04-2005

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Orion Corporation

    Finland
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    Ciprofloxacin Hydrochloride Anhydrous

    Brand Name : Ciprofloxacin \"Orion\"

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 21-11-2016

    Application Number : 28105813516

    Regulatory Info : Prescription

    Registration Country : Denmark

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    Orion Corporation

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    Regulatory Info : Prescription

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    Ciprofloxacin Hydrochloride Anhydrous

    Brand Name : Ciprofloxacin \"Orion\"

    Dosage Form : Film Coated Tablet

    Dosage Strength : 750mg

    Packaging :

    Approval Date : 21-11-2016

    Application Number : 28105813616

    Regulatory Info : Prescription

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    Orion Corporation

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    Regulatory Info : Approved

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    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Ciprofloxacin Orion

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250mg

    Packaging :

    Approval Date : 25-11-2016

    Application Number : 2.02E+13

    Regulatory Info : Approved

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