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    01 2ABBVIE

    02 1STRIDES PHARMA

    03 1ABON PHARMS LLC

    04 1AMNEAL

    05 1AMNEAL PHARMS

    06 1CHARTWELL RX

    07 1COSETTE

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    01

    ABBVIE

    U.S.A
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    Europ. Pharma Outsourcing
    Not Confirmed
    • fda
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    RLD : Yes

    TE Code : AB

    SUCRALFATE

    Brand Name : CARAFATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1GM

    Approval Date : 1982-01-01

    Application Number : 18333

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    02

    STRIDES PHARMA

    India
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    CPhI WW Frankfurt
    Booth # 9.1F6 & 9.1G41
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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 2024-05-21

    Application Number : 216474

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

    Strides Pharma Science

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    03

    ABBVIE

    U.S.A
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    Europ. Pharma Outsourcing
    Not Confirmed
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    RLD : Yes

    TE Code : AB

    SUCRALFATE

    Brand Name : CARAFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 1993-12-16

    Application Number : 19183

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    04

    AMNEAL

    U.S.A
    Europ. Pharma Outsourcing
    Not Confirmed
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    AMNEAL

    U.S.A
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    Europ. Pharma Outsourcing
    Not Confirmed
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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 2019-12-02

    Application Number : 209356

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    CHARTWELL RX

    U.S.A
    Europ. Pharma Outsourcing
    Not Confirmed
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    CHARTWELL RX

    U.S.A
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    Europ. Pharma Outsourcing
    Not Confirmed
    • fda
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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1GM

    Approval Date : 1998-06-08

    Application Number : 74415

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    HIKMA

    United Kingdom
    Europ. Pharma Outsourcing
    Not Confirmed
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    HIKMA

    United Kingdom
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    Europ. Pharma Outsourcing
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code :

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 2024-07-23

    Application Number : 212769

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    PADAGIS US

    Israel
    Europ. Pharma Outsourcing
    Not Confirmed
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    PADAGIS US

    Israel
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    Europ. Pharma Outsourcing
    Not Confirmed
    • fda
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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 2025-04-14

    Application Number : 211780

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    TEVA

    Israel
    Europ. Pharma Outsourcing
    Not Confirmed
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    TEVA

    Israel
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    Europ. Pharma Outsourcing
    Not Confirmed
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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1GM

    Approval Date : 1996-03-29

    Application Number : 70848

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    MYLAN

    U.S.A
    Europ. Pharma Outsourcing
    Not Confirmed
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    MYLAN

    U.S.A
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    Europ. Pharma Outsourcing
    Not Confirmed
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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 2022-09-12

    Application Number : 212913

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    VISTAPHARM LLC

    India
    Europ. Pharma Outsourcing
    Not Confirmed
    arrow

    VISTAPHARM LLC

    India
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    Europ. Pharma Outsourcing
    Not Confirmed
    • fda
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    RLD : No

    TE Code : AB

    SUCRALFATE

    Brand Name : SUCRALFATE

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 1GM/10ML

    Approval Date : 2022-03-15

    Application Number : 211884

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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