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    Areva Pharmaceuticals

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    01 2CASPOFUNGIN ACETATE

    02 1FLUDARABINE PHOSPHATE

    03 1FUROSEMIDE

    04 3PAMIDRONATE DISODIUM

    05 1TERBUTALINE SULFATE

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    01

    Brand Name : CASPOFUNGIN ACETATE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : CASPOFUNGIN ACETATE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    RLD : No

    TE Code : AP

    CASPOFUNGIN ACETATE

    Areva Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : CASPOFUNGIN ACETATE

    Dosage Strength : 50MG/VIAL

    Approval Date : 2021-10-01

    Application Number : 211263

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : CASPOFUNGIN ACETATE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : CASPOFUNGIN ACETATE

    U.S.A
    Pharmtech & Ingredients
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    RLD : No

    TE Code : AP

    CASPOFUNGIN ACETATE

    Areva Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : CASPOFUNGIN ACETATE

    Dosage Strength : 70MG/VIAL

    Approval Date : 2021-10-01

    Application Number : 211263

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : FLUDARABINE PHOSPHAT...

    U.S.A
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    Brand Name : FLUDARABINE PHOSPHAT...

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    RLD : No

    TE Code : AP1

    FLUDARABINE PHOSPHATE

    Areva Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : FLUDARABINE PHOSPHATE

    Dosage Strength : 50MG/2ML (25MG/ML)

    Approval Date : 2010-09-27

    Application Number : 90724

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP1

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    04

    Brand Name : FUROSEMIDE

    U.S.A
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    Brand Name : FUROSEMIDE

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    RLD : No

    TE Code : AP

    FUROSEMIDE

    Areva Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : FUROSEMIDE

    Dosage Strength : 10MG/ML

    Approval Date : 2020-12-18

    Application Number : 208435

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    Brand Name : PAMIDRONATE DISODIUM

    U.S.A
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    Not Confirmed
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    Brand Name : PAMIDRONATE DISODIUM

    U.S.A
    Pharmtech & Ingredients
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    RLD : No

    TE Code : AP

    PAMIDRONATE DISODIUM

    Areva Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : PAMIDRONATE DISODIUM

    Dosage Strength : 30MG/VIAL

    Approval Date : 2008-11-26

    Application Number : 77433

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    Brand Name : PAMIDRONATE DISODIUM

    U.S.A
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    Not Confirmed
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    Brand Name : PAMIDRONATE DISODIUM

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    Pharmtech & Ingredients
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    RLD : No

    TE Code :

    PAMIDRONATE DISODIUM

    Areva Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : PAMIDRONATE DISODIUM

    Dosage Strength : 60MG/VIAL

    Approval Date : 2008-11-26

    Application Number : 77433

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    Brand Name : PAMIDRONATE DISODIUM

    U.S.A
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    Not Confirmed
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    Brand Name : PAMIDRONATE DISODIUM

    U.S.A
    Pharmtech & Ingredients
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    • EDQM
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    RLD : No

    TE Code : AP

    PAMIDRONATE DISODIUM

    Areva Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : PAMIDRONATE DISODIUM

    Dosage Strength : 90MG/VIAL

    Approval Date : 2008-11-26

    Application Number : 77433

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    08

    Brand Name : TERBUTALINE SULFATE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : TERBUTALINE SULFATE

    U.S.A
    Pharmtech & Ingredients
    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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    Virtual Booth Virtual Booth
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    RLD : No

    TE Code : AP

    TERBUTALINE SULFATE

    Areva Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : TERBUTALINE SULFATE

    Dosage Strength : 1MG/ML

    Approval Date : 2013-11-08

    Application Number : 200122

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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