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    Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.

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    Meglumine sodium amidotrizoate injection

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    Biophore India Pharmaceuticals Pvt ...

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

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    Diatrizoate Sodium

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    Diatrizoate Sodium; Diatrizoate Meglumine

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    Amphastar Pharmaceuticals

    U.S.A
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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : DIATRIZOATE-60

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 52%;8%

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    Approval Date : 1983-06-17

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    ANDA Repository

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    Brand Name : DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM

    Dosage Form : SOLUTION;ORAL, RECTAL

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    Annora Pharma

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    Dosage Form : SOLUTION;ORAL, RECTAL

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    Approval Date : 2023-11-17

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    Bayer AG

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : ANGIOVIST 370

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    Approval Date : 1982-09-23

    Application Number : 87723

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    Bayer AG

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : ANGIOVIST 292

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    Approval Date : 1982-09-23

    Application Number : 87724

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    Bayer AG

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    DIATRIZOATE SODIUM

    Brand Name : UROVIST SODIUM 300

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    Approval Date : 1982-09-23

    Application Number : 87725

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    Bayer AG

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    Brand Name : GASTROVIST

    Dosage Form : SOLUTION;ORAL, RECTAL

    Dosage Strength : 66%;10%

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    Approval Date : 1982-09-23

    Application Number : 87728

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    Bracco

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : RENOGRAFIN-76

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 66%;10%

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    Approval Date : 1982-01-01

    Application Number : 10040

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    Bracco

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : RENOGRAFIN-60

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 52%;8%

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    Approval Date : 1982-01-01

    Application Number : 10040

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    Bracco

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : RENOVIST II

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 28.5%;29.1%

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    Approval Date : 1982-01-01

    Application Number : 10040

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    13

    Bracco

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : RENOVIST

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 34.3%;35%

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    Approval Date : 1982-01-01

    Application Number : 10040

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    14

    Bracco

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : GASTROGRAFIN

    Dosage Form : SOLUTION;ORAL, RECTAL

    Dosage Strength : 66%;10%

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    Approval Date : 1982-01-01

    Application Number : 11245

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    Bracco

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : RENOCAL-76

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 66%;10%

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    Approval Date : 1988-06-01

    Application Number : 89347

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    GE Healthcare Inc

    United Kingdom
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    GE Healthcare Inc

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    DIATRIZOATE SODIUM

    Brand Name : HYPAQUE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50%

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    Approval Date : 1982-01-01

    Application Number : 9561

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    GE Healthcare Inc

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    DIATRIZOATE SODIUM

    Brand Name : HYPAQUE SODIUM 20%

    Dosage Form : SOLUTION;URETERAL

    Dosage Strength : 20%

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    Approval Date : 1982-01-01

    Application Number : 9561

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    GE Healthcare Inc

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    DIATRIZOATE SODIUM

    Brand Name : HYPAQUE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25%

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    Approval Date : 1982-01-01

    Application Number : 9561

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    GE Healthcare Inc

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : HYPAQUE-M,90%

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 60%;30%

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    Approval Date : 1982-01-01

    Application Number : 10220

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    GE Healthcare Inc

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : HYPAQUE-M,75%

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50%;25%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 10220

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    GE Healthcare Inc

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    DIATRIZOATE SODIUM

    Brand Name : HYPAQUE

    Dosage Form : FOR SOLUTION;ORAL, RECTAL

    Dosage Strength : 100%

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    Approval Date : 1982-01-01

    Application Number : 11386

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    GE Healthcare Inc

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    DIATRIZOATE SODIUM

    Brand Name : HYPAQUE

    Dosage Form : SOLUTION;ORAL, RECTAL

    Dosage Strength : 40%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11386

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    GE Healthcare Inc

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : HYPAQUE-76

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 66%;10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86505

    Regulatory Info : DISCN

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    Mallinckrodt Pharmaceuticals

    Ireland
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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : MD-76R

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 66%;10%

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    Approval Date : 1989-09-29

    Application Number : 19292

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    Mallinckrodt Pharmaceuticals

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    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : MD-76

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 66%;10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87073

    Regulatory Info : DISCN

    Registration Country : USA

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    Mallinckrodt Pharmaceuticals

    Ireland
    VMX
    Not Confirmed
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    Mallinckrodt Pharmaceuticals

    Ireland
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    VMX
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    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : MD-60

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 52%;8%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87074

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Mallinckrodt Pharmaceuticals

    Ireland
    VMX
    Not Confirmed
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    Mallinckrodt Pharmaceuticals

    Ireland
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    VMX
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    DIATRIZOATE SODIUM

    Brand Name : MD-50

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87075

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Mallinckrodt Pharmaceuticals

    Ireland
    VMX
    Not Confirmed
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    Mallinckrodt Pharmaceuticals

    Ireland
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    VMX
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    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    Brand Name : MD-GASTROVIEW

    Dosage Form : SOLUTION;ORAL, RECTAL

    Dosage Strength : 66%;10%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87388

    Regulatory Info : RX

    Registration Country : USA

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