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    01 1Zenara Pharma

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    01

    Zenara Pharma

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

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    Approval Date : 2025-06-11

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    Dr. Reddy's Laboratories

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

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    Dosage Strength : 100MG

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    Approval Date : 2021-06-15

    Application Number : 207685

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    Aucta Pharmaceuticals

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : ZELVYSIA

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    Dosage Strength : 100MG/PACKET

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    Approval Date : 2025-04-29

    Application Number : 218645

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    Dr. Reddy's Laboratories

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

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    Dosage Strength : 100MG/PACKET

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    Approval Date : 2021-03-30

    Application Number : 209452

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    05

    Dr. Reddy's Laboratories

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 500MG/PACKET

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    Approval Date : 2022-05-13

    Application Number : 215798

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    06

    Dr. Reddy's Laboratories

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : REDDY-SAPROPTERIN

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 100MG/SACHET

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    Application Number : 2534533

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    07

    Dr. Reddy's Laboratories

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    SAPROPTERIN DIHYDROCHLORIDE

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    Application Number : 2535610

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    Aucta Pharmaceuticals

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : ZELVYSIA

    Dosage Form : POWDER;ORAL

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    Approval Date : 2025-04-29

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    09

    Annora Pharma

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 100MG/PACKET

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    Approval Date : 2022-08-18

    Application Number : 215420

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    10

    Annora Pharma

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 500MG/PACKET

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    Approval Date : 2022-08-18

    Application Number : 215420

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    11

    Annora Pharma

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

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    Approval Date : 2022-08-23

    Application Number : 215534

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    12

    Aurobindo Pharma Limited

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

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    Approval Date : 2025-06-09

    Application Number : 216797

    Regulatory Info : RX

    Registration Country : USA

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    13

    BioMarin Pharmaceutical

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : KUVAN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

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    Approval Date : 2007-12-13

    Application Number : 22181

    Regulatory Info : RX

    Registration Country : USA

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    14

    BioMarin Pharmaceutical

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    Brand Name : KUVAN

    Dosage Form : POWDER;ORAL

    Dosage Strength : 100MG/PACKET

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    Approval Date : 2013-12-19

    Application Number : 205065

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    15

    BioMarin Pharmaceutical

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    Brand Name : KUVAN

    Dosage Form : POWDER;ORAL

    Dosage Strength : 500MG/PACKET

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    Approval Date : 2015-10-27

    Application Number : 205065

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    PH HEALTH

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    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 2019-05-10

    Application Number : 207200

    Regulatory Info : RX

    Registration Country : USA

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    17

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    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 100MG/PACKET

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    Approval Date : 2019-08-20

    Application Number : 207207

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    PH HEALTH

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    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 500MG/PACKET

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    Approval Date : 2019-08-20

    Application Number : 210027

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    HOPEWELL PHARMA

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    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 100MG/PACKET

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    Approval Date : 2025-09-03

    Application Number : 216432

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    Registration Country : USA

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    20

    HOPEWELL PHARMA

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    SAPROPTERIN DIHYDROCHLORIDE

    Brand Name : SAPROPTERIN DIHYDROCHLORIDE

    Dosage Form : POWDER;ORAL

    Dosage Strength : 500MG/PACKET

    Packaging :

    Approval Date : 2025-09-03

    Application Number : 216432

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    Registration Country : USA

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