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    AstraZeneca

    United Kingdom
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    OMEPRAZOLE MAGNESIUM

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    Approval Date : 2003-06-20

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    omeprazole magnesium

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    Brand Name : Losecpro

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    Aurobindo Pharma Limited

    India
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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

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    Approval Date : 2018-06-06

    Application Number : 206877

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    Aurobindo Pharma Limited

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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : CAPSULE, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

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    Approval Date : 2023-04-28

    Application Number : 213201

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    Covis Pharma

    Luxembourg
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    OMEPRAZOLE MAGNESIUM

    Brand Name : PRILOSEC

    Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 2.5MG BASE/PACKET

    Packaging :

    Approval Date : 2008-03-20

    Application Number : 22056

    Regulatory Info : RX

    Registration Country : USA

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    10

    Covis Pharma

    Luxembourg
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    OMEPRAZOLE MAGNESIUM

    Brand Name : PRILOSEC

    Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 10MG BASE/PACKET

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    Approval Date : 2008-03-20

    Application Number : 22056

    Regulatory Info : RX

    Registration Country : USA

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    11

    Hetero Drugs

    India
    AMWC Asia-TDAC
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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2020-03-25

    Application Number : 211732

    Regulatory Info : OTC

    Registration Country : USA

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    12

    ORIFARM GROUP AS

    Denmark
    AMWC Asia-TDAC
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    Denmark
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    Brand Name : Losec MUPS

    Dosage Form : GASTRO

    Dosage Strength : 20 MG

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    ORIFARM GROUP AS

    Denmark
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    Denmark
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    Brand Name : Losec MUPS

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    Dosage Strength : 20 MG

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    14

    Perrigo Company plc

    Ireland
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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2015-07-30

    Application Number : 204152

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Perrigo Company plc

    Ireland
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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : CAPSULE, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2022-05-24

    Application Number : 216096

    Regulatory Info : OTC

    Registration Country : USA

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    16

    Pharmascience Inc.

    Canada
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    Omeprazole Magnesium

    Brand Name : PMS-OMEPRAZOLE DR

    Dosage Form : TABLET (DELAYED-RELEASE)

    Dosage Strength : 10MG

    Packaging : 30/100

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    Regulatory Info : Prescription

    Registration Country : Canada

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    17

    PL Developments

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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2020-06-01

    Application Number : 206582

    Regulatory Info : OTC

    Registration Country : USA

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    18

    RedHill Biopharma

    Israel
    AMWC Asia-TDAC
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    Israel
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    AMOXICILLIN; OMEPRAZOLE MAGNESIUM; RIFABUTIN

    Brand Name : TALICIA

    Dosage Form : CAPSULE, DELAYED RELEASE;ORAL

    Dosage Strength : 250MG;EQ 10MG BASE;12.5MG

    Packaging :

    Approval Date : 2019-11-01

    Application Number : 213004

    Regulatory Info : RX

    Registration Country : USA

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    19

    Spil

    Taiwan
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    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : CAPSULE, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2018-07-20

    Application Number : 210593

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    XYZ Pharma

    Gabon
    AMWC Asia-TDAC
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    Gabon
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    Regulatory Info : OTC

    Registration Country : USA

    OMEPRAZOLE MAGNESIUM

    Brand Name : OMEPRAZOLE MAGNESIUM

    Dosage Form : CAPSULE, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2009-06-05

    Application Number : 78878

    Regulatory Info : OTC

    Registration Country : USA

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