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

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    Caffeine Citrate

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    01 2AM REGENT

    02 1EUGIA PHARMA

    03 1EXELA PHARMA

    04 1EXELA PHARMA SCIENCE

    05 2FRESENIUS KABI USA

    06 2HIKMA

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    01

    AM REGENT

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    AM REGENT

    U.S.A
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    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code : AP

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2007-05-15

    Application Number : 77906

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    AM REGENT

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    AM REGENT

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code :

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2009-11-20

    Application Number : 90064

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    EXELA PHARMA SCIENCE

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    EXELA PHARMA SCIENCE

    U.S.A
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    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code : AP

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2006-09-21

    Application Number : 77233

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    04

    EXELA PHARMA

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    EXELA PHARMA

    U.S.A
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    The Generic Rx Session
    Not Confirmed
    • fda
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    RLD : No

    TE Code : AA

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2006-09-21

    Application Number : 77304

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    05

    FRESENIUS KABI USA

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    FRESENIUS KABI USA

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AP

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2007-07-20

    Application Number : 77997

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    06

    FRESENIUS KABI USA

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    FRESENIUS KABI USA

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • 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 : AA

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2008-01-31

    Application Number : 78002

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    07

    HIKMA

    United Kingdom
    The Generic Rx Session
    Not Confirmed
    arrow

    HIKMA

    United Kingdom
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
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    RLD : Yes

    TE Code : AP

    CAFFEINE CITRATE

    Brand Name : CAFCIT

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 1999-09-21

    Application Number : 20793

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    08

    HIKMA

    United Kingdom
    The Generic Rx Session
    Not Confirmed
    arrow

    HIKMA

    United Kingdom
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    CAFFEINE CITRATE

    Brand Name : CAFCIT

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2000-04-12

    Application Number : 20793

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    SUN PHARM

    India
    The Generic Rx Session
    Not Confirmed
    arrow

    SUN PHARM

    India
    arrow
    The Generic Rx Session
    Not Confirmed
    • 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 :

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2009-09-30

    Application Number : 90077

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    SUN PHARM

    India
    The Generic Rx Session
    Not Confirmed
    arrow

    SUN PHARM

    India
    arrow
    The Generic Rx Session
    Not Confirmed
    • 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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    Flag India
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    RLD : No

    TE Code : AA

    CAFFEINE CITRATE

    Brand Name : CAFFEINE CITRATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

    Approval Date : 2009-09-30

    Application Number : 90357

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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