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    Approved Drug Products containing Altana Pharma brand of alfuzosin hydrochloride listed in the FDA Orange Book. Original Data : FDA Website

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    Altana Pharma brand of alfuzosin hydrochloride

    ACTIVE PHARMA INGREDIENTS

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    01 1APOTEX INC

    02 1AUROBINDO PHARMA LTD

    03 1CHARTWELL RX

    04 1CONCORDIA

    05 1INVAGEN PHARMS

    06 1NORVIUM BIOSCIENCE

    07 1SUN PHARM

    08 1TORRENT PHARMS

    09 1UNICHEM

    10 1WOCKHARDT

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    01

    APOTEX INC

    Canada
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    APOTEX INC

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    RLD : No

    TE Code : AB

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2011-07-18

    Application Number : 79013

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    AUROBINDO PHARMA LTD

    India
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    RLD : No

    TE Code : AB

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2012-08-30

    Application Number : 79060

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    CHARTWELL RX

    U.S.A
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    RLD : No

    TE Code :

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2011-07-18

    Application Number : 79056

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    CONCORDIA

    United Kingdom
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    RLD : Yes

    TE Code : AB

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : UROXATRAL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2003-06-12

    Application Number : 21287

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    05

    INVAGEN PHARMS

    U.S.A
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    RLD : No

    TE Code : AB

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2012-01-17

    Application Number : 90284

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    SUN PHARM

    India
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    RLD : No

    TE Code : AB

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2011-07-18

    Application Number : 79057

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    TORRENT PHARMS

    India
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    TORRENT PHARMS

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    RLD : No

    TE Code :

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2011-07-18

    Application Number : 79054

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    UNICHEM

    U.S.A
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    RLD : No

    TE Code : AB

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2016-01-28

    Application Number : 203192

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    WOCKHARDT

    India
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    RLD : No

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    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2012-08-10

    Application Number : 90221

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    NORVIUM BIOSCIENCE

    Country
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    RLD : No

    TE Code :

    ALFUZOSIN HYDROCHLORIDE

    Brand Name : ALFUZOSIN HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Approval Date : 2011-07-18

    Application Number : 79014

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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