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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Rabeprazole Sodium

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    01 1DR REDDYS

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    03 1AMNEAL PHARMS

    04 1AUROBINDO PHARMA

    05 2AYTU

    06 1CHARTWELL RX

    07 1EISAI MEDCL RES

    08 1LANNETT CO INC

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    01

    DR REDDYS

    India
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    RLD : No

    TE Code : AB

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2013-11-08

    Application Number : 76824

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    AMNEAL PHARMS

    U.S.A
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    AMNEAL PHARMS

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    RLD : No

    TE Code : AB

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2015-07-31

    Application Number : 204179

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    CHARTWELL RX

    U.S.A
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    RLD : No

    TE Code : AB

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2013-11-08

    Application Number : 78964

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    EISAI MEDCL RES

    Japan
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    RLD :

    TE Code :

    RABEPRAZOLE SODIUM

    Brand Name : ACIPHEX

    Dosage Form : Tablet, Delayed Release; Oral

    Dosage Strength : 20MG

    Approval Date :

    Application Number : 21456

    RX/OTC/DISCN :

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    TE Code :

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    05

    LANNETT CO INC

    U.S.A
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    LANNETT CO INC

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    RLD : No

    TE Code : AB

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2013-11-08

    Application Number : 90678

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    TEVA PHARMS USA

    Israel
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    TEVA PHARMS USA

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    RLD : No

    TE Code :

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2013-11-08

    Application Number : 76822

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    TORRENT

    India
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    TORRENT

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    RLD : No

    TE Code : AB

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2013-11-08

    Application Number : 202376

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    WAYLIS THERAP

    U.S.A
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    WAYLIS THERAP

    U.S.A
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    RLD : Yes

    TE Code :

    RABEPRAZOLE SODIUM

    Brand Name : ACIPHEX

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2002-05-29

    Application Number : 20973

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    WAYLIS THERAP

    U.S.A
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    WAYLIS THERAP

    U.S.A
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    RLD : Yes

    TE Code : AB

    RABEPRAZOLE SODIUM

    Brand Name : ACIPHEX

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 1999-08-19

    Application Number : 20973

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    10

    NORVIUM BIOSCIENCE

    Country
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    NORVIUM BIOSCIENCE

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    RLD : No

    TE Code :

    RABEPRAZOLE SODIUM

    Brand Name : RABEPRAZOLE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 20MG

    Approval Date : 2013-11-08

    Application Number : 76885

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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