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    Approved Drug Products of Qingdao Baheal Pharmaceutical listed in the FDA Orange Book. Original Data : FDA Website

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Qingdao BAHEAL pharmaceutical

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    01 4CELECOXIB

    02 3DULOXETINE HYDROCHLORIDE

    03 1FOLIC ACID

    04 2METFORMIN HYDROCHLORIDE

    05 4METHIMAZOLE

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    01

    Brand Name : CELECOXIB

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : CELECOXIB

    China
    Discovery on Target
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    RLD : No

    TE Code : AB

    CELECOXIB

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CELECOXIB

    Dosage Strength : 50MG

    Approval Date : 2019-08-07

    Application Number : 208856

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : CELECOXIB

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : CELECOXIB

    China
    Discovery on Target
    Not Confirmed
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    RLD : No

    TE Code : AB

    CELECOXIB

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CELECOXIB

    Dosage Strength : 100MG

    Approval Date : 2019-08-07

    Application Number : 208856

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : CELECOXIB

    China
    Discovery on Target
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    Brand Name : CELECOXIB

    China
    Discovery on Target
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    RLD : No

    TE Code : AB

    CELECOXIB

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CELECOXIB

    Dosage Strength : 200MG

    Approval Date : 2019-08-07

    Application Number : 208856

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : CELECOXIB

    China
    Discovery on Target
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    Brand Name : CELECOXIB

    China
    Discovery on Target
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    RLD : No

    TE Code : AB

    CELECOXIB

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CELECOXIB

    Dosage Strength : 400MG

    Approval Date : 2019-08-07

    Application Number : 208856

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : DULOXETINE HYDROCHLO...

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : DULOXETINE HYDROCHLO...

    China
    Discovery on Target
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    RLD : No

    TE Code : AB

    DULOXETINE HYDROCHLORIDE

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE, DELAYED REL PELLETS; ...

    Proprietary Name : DULOXETINE HYDROCHLORIDE

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2019-04-17

    Application Number : 210599

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : DULOXETINE HYDROCHLO...

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : DULOXETINE HYDROCHLO...

    China
    Discovery on Target
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    DULOXETINE HYDROCHLORIDE

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE, DELAYED REL PELLETS; ...

    Proprietary Name : DULOXETINE HYDROCHLORIDE

    Dosage Strength : EQ 30MG BASE

    Approval Date : 2019-04-17

    Application Number : 210599

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : DULOXETINE HYDROCHLO...

    China
    Discovery on Target
    Not Confirmed
    arrow

    Brand Name : DULOXETINE HYDROCHLO...

    China
    Discovery on Target
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
    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 : AB

    DULOXETINE HYDROCHLORIDE

    Qingdao BAHEAL pharmaceutical

    Dosage Form : CAPSULE, DELAYED REL PELLETS; ...

    Proprietary Name : DULOXETINE HYDROCHLORIDE

    Dosage Strength : EQ 60MG BASE

    Approval Date : 2019-04-17

    Application Number : 210599

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Market
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    08

    Brand Name : FOLIC ACID

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : FOLIC ACID

    China
    Discovery on Target
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AA

    FOLIC ACID

    Qingdao BAHEAL pharmaceutical

    Dosage Form : TABLET; ORAL

    Proprietary Name : FOLIC ACID

    Dosage Strength : 1MG

    Approval Date : 2013-07-12

    Application Number : 91145

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    09

    Brand Name : METFORMIN HYDROCHLOR...

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : METFORMIN HYDROCHLOR...

    China
    Discovery on Target
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB2

    METFORMIN HYDROCHLORIDE

    Qingdao BAHEAL pharmaceutical

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : METFORMIN HYDROCHLORIDE

    Dosage Strength : 500MG

    Approval Date : 2018-12-27

    Application Number : 209993

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB2

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    10

    Brand Name : METFORMIN HYDROCHLOR...

    China
    Discovery on Target
    Not Confirmed
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    Brand Name : METFORMIN HYDROCHLOR...

    China
    Discovery on Target
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
    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 : AB2

    METFORMIN HYDROCHLORIDE

    Qingdao BAHEAL pharmaceutical

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : METFORMIN HYDROCHLORIDE

    Dosage Strength : 1GM

    Approval Date : 2018-12-27

    Application Number : 209993

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB2

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