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    Ciprofloxacin Monohydrochloride Monohydrate

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    01 1Aspen Pharmacare Holdings

    02 3Orion Corporation

    03 2Towa Pharmaceutical

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    01

    Aspen Pharmacare Holdings

    South Africa
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    Regulatory Info : Generic

    Registration Country : South Africa

    Ciprofloxacin Hydrochloride Monohydrate

    Brand Name : Otixal

    Dosage Form : EAR

    Dosage Strength : 3mg

    Packaging : 10X1mg

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Africa

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    02

    Orion Corporation

    Finland
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    Regulatory Info : Approved

    Registration Country : Sweden

    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Ciprofloxacin Orion

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250mg

    Packaging :

    Approval Date : 25/11/2016

    Application Number : 20160705000034

    Regulatory Info : Approved

    Registration Country : Sweden

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    03

    Towa Pharmaceutical

    Japan
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    Regulatory Info : Suspended

    Registration Country : Spain

    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Think

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 21-03-2000

    Application Number : 62962

    Regulatory Info : Suspended

    Registration Country : Spain

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    04

    Orion Corporation

    Finland
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    Regulatory Info : Approved

    Registration Country : Sweden

    Ciprofloxacin Hydrochloride (Monohydrate)

    Brand Name : Ciprofloxacin Orion

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500mg

    Packaging :

    Approval Date : 25/11/2016

    Application Number : 20160705000041

    Regulatory Info : Approved

    Registration Country : Sweden

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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 : 750mg

    Packaging :

    Approval Date : 25/11/2016

    Application Number : 20160705000058

    Regulatory Info : Approved

    Registration Country : Sweden

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    06

    Towa Pharmaceutical

    Japan
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    Regulatory Info : Authorized

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    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Think

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 01-08-1999

    Application Number : 62709

    Regulatory Info : Authorized

    Registration Country : Spain

    Towa Pharmaceutical

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    07

    Bayer AG

    Germany
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    Regulatory Info : RX

    Registration Country : USA

    CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CIPRO

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 1987-10-22

    Application Number : 19537

    Regulatory Info : RX

    Registration Country : USA

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    08

    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

    Packaging :

    Approval Date : 1987-10-22

    Application Number : 19537

    Regulatory Info : RX

    Registration Country : USA

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    09

    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1987-10-22

    Application Number : 19537

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 2002-12-13

    Application Number : 21473

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Sandoz B2B

    Switzerland
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    Switzerland
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    Regulatory Info : RX

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    CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CILOXAN

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.3% BASE

    Packaging :

    Approval Date : 1990-12-31

    Application Number : 19992

    Regulatory Info : RX

    Registration Country : USA

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    Sandoz B2B

    Switzerland
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    CIPROFLOXACIN HYDROCHLORIDE

    Brand Name : CILOXAN

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 0.3% BASE

    Packaging :

    Approval Date : 1998-03-30

    Application Number : 20369

    Regulatory Info : RX

    Registration Country : USA

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    Sandoz B2B

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    Regulatory Info : RX

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    CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE

    Brand Name : CIPRO HC

    Dosage Form : SUSPENSION/DROPS;OTIC

    Dosage Strength : EQ 0.2% BASE;1%

    Packaging :

    Approval Date : 1998-02-10

    Application Number : 20805

    Regulatory Info : RX

    Registration Country : USA

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    Azure Pharmaceuticals Ltd

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    Regulatory Info : Withdrawn

    Registration Country : Malta

    Ciprofloxacin Hydrochloride

    Brand Name : Ciplox

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2020-09-29

    Application Number :

    Regulatory Info : Withdrawn

    Registration Country : Malta

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    NeoFarma Pharmaceuticals Limited

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    Regulatory Info : Authorised

    Registration Country : Malta

    Ciprofloxacin Hydrochloride

    Brand Name : Ciproxin

    Dosage Form : Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2021-01-21

    Application Number :

    Regulatory Info : Authorised

    Registration Country : Malta

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    Azure Pharmaceuticals Ltd

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    Regulatory Info : Authorised

    Registration Country : Malta

    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Teva

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2023-10-18

    Application Number :

    Regulatory Info : Authorised

    Registration Country : Malta

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    NeoFarma Pharmaceuticals Limited

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    Regulatory Info : Authorised

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    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Teva

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 2024-10-18

    Application Number :

    Regulatory Info : Authorised

    Registration Country : Malta

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    NeoFarma Pharmaceuticals Limited

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    Brand Name : Ciprofloxacin Teva

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    Approval Date : 2024-10-18

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    Regulatory Info : Authorised

    Registration Country : Malta

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    Central Procurement & Supplies Unit

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    Regulatory Info : Authorised

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    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacino Cinfa

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 2025-08-14

    Application Number :

    Regulatory Info : Authorised

    Registration Country : Malta

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    NM Pharma Limited

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    Ciprofloxacin Hydrochloride

    Brand Name : Ciprofloxacin Viatris

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2025-08-18

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    Regulatory Info : Authorised

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