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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    04 1SODIUM FLUORIDE F-18

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    Brand Name : AMMONIA N 13

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    Brand Name : AMMONIA N 13

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    Regulatory Info : RX

    Registration Country : USA

    AMMONIA N-13

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    Dosage Form : INJECTABLE;INTRAVENOUS

    Brand Name : AMMONIA N 13

    Dosage Strength : 30mCi-300mCi/8ML (3.75...

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    Approval Date : 2007-08-23

    Application Number : 22119

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FLUDEOXYGLUCOSE F18

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    Brand Name : FLUDEOXYGLUCOSE F18

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    Regulatory Info : DISCN

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    FLUDEOXYGLUCOSE F-18

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    Dosage Form : INJECTABLE;INTRAVENOUS

    Brand Name : FLUDEOXYGLUCOSE F18

    Dosage Strength : 20-200mCi/ML **Federal...

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    Approval Date : 2005-08-19

    Application Number : 21870

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : FLUDEOXYGLUCOSE F18

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    Brand Name : FLUDEOXYGLUCOSE F18

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    FLUDEOXYGLUCOSE F-18

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    Dosage Form : INJECTABLE;INTRAVENOUS

    Brand Name : FLUDEOXYGLUCOSE F18

    Dosage Strength : 20-400mCi/ML

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    Approval Date : 2008-11-21

    Application Number : 21870

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    Registration Country : USA

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    Brand Name : FLUORODOPA F18

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    Regulatory Info : RX

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    FLUORODOPA F-18

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    Dosage Form : SOLUTION;INTRAVENOUS

    Brand Name : FLUORODOPA F18

    Dosage Strength : 0.42-8.33mCi/ML

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    Approval Date : 2019-10-10

    Application Number : 200655

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : SODIUM FLUORIDE F-18

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    Brand Name : SODIUM FLUORIDE F-18

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    Regulatory Info : RX

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    SODIUM FLUORIDE F-18

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    Dosage Form : INJECTABLE;INTRAVENOUS

    Brand Name : SODIUM FLUORIDE F-18

    Dosage Strength : 20-600mCi/ML

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    Approval Date : 2014-11-19

    Application Number : 204328

    Regulatory Info : RX

    Registration Country : USA

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