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    Anagrelide Hydrochloride

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    01

    WATSON LABS

    Ireland
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    WATSON LABS

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    RLD : No

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

    Approval Date : 2005-04-18

    Application Number : 76417

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    WATSON LABS

    Ireland
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    RLD : No

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE

    Approval Date : 2005-04-18

    Application Number : 76417

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

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    05

    ROXANE

    U.S.A
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    ROXANE

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    RLD : No

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

    Approval Date : 2005-04-18

    Application Number : 76489

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    ROXANE

    U.S.A
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    RLD : No

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE

    Approval Date : 2005-04-18

    Application Number : 76489

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    TAKEDA PHARMS USA

    Japan
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    TAKEDA PHARMS USA

    Japan
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    RLD : No

    TE Code : AB

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : AGRYLIN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

    Approval Date : 1997-03-14

    Application Number : 20333

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    TAKEDA PHARMS USA

    Japan
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    TAKEDA PHARMS USA

    Japan
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    ChemOutsourcing
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    RLD : Yes

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : AGRYLIN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1997-03-14

    Application Number : 20333

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    BARR LABS

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    RLD : No

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

    Approval Date : 2005-04-18

    Application Number : 76530

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    BARR LABS

    Country
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    BARR LABS

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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : No

    TE Code :

    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE

    Approval Date : 2005-04-18

    Application Number : 76530

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

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