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    01 6Actavis Inc

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    01

    Actavis Inc

    Ireland
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    METHYLPREDNISOLONE ACETATE

    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

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    Approval Date : 1982-01-01

    Application Number : 85374

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    Registration Country : USA

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    02

    Actavis Inc

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    METHYLPREDNISOLONE ACETATE

    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/ML

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    Approval Date : 1982-01-01

    Application Number : 85595

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Actavis Inc

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    METHYLPREDNISOLONE ACETATE

    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

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    Approval Date : 1982-01-01

    Application Number : 85597

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Actavis Inc

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    METHYLPREDNISOLONE ACETATE

    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85600

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Pfizer Inc

    U.S.A
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    METHYLPREDNISOLONE ACETATE

    Brand Name : DEPO-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11757

    Regulatory Info : RX

    Registration Country : USA

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    06

    Pfizer Inc

    U.S.A
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    Regulatory Info : RX

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    METHYLPREDNISOLONE ACETATE

    Brand Name : DEPO-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11757

    Regulatory Info : RX

    Registration Country : USA

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    07

    Pfizer Inc

    U.S.A
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    METHYLPREDNISOLONE ACETATE

    Brand Name : DEPO-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11757

    Regulatory Info : RX

    Registration Country : USA

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    08

    Pfizer Inc

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    METHYLPREDNISOLONE ACETATE

    Brand Name : MEDROL ACETATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.25%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12421

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

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    METHYLPREDNISOLONE ACETATE

    Brand Name : MEDROL ACETATE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 1%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12421

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Pfizer Inc

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    Regulatory Info : DISCN

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    METHYLPREDNISOLONE ACETATE

    Brand Name : MEDROL

    Dosage Form : ENEMA;RECTAL

    Dosage Strength : 40MG/BOT

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18102

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

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    METHYLPREDNISOLONE ACETATE; NEOMYCIN SULFATE

    Brand Name : NEO-MEDROL ACETATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 60611

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

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    METHYLPREDNISOLONE ACETATE; NEOMYCIN SULFATE

    Brand Name : NEO-MEDROL ACETATE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.25%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 60611

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Sandoz B2B

    Switzerland
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    Switzerland
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    Regulatory Info : RX

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    METHYLPREDNISOLONE ACETATE

    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 2009-01-29

    Application Number : 40719

    Regulatory Info : RX

    Registration Country : USA

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    14

    Sandoz B2B

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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/ML

    Packaging :

    Approval Date : 2009-01-29

    Application Number : 40719

    Regulatory Info : RX

    Registration Country : USA

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    Sandoz B2B

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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 2009-03-05

    Application Number : 40794

    Regulatory Info : RX

    Registration Country : USA

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    16

    Sandoz B2B

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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/ML

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    Approval Date : 2009-03-05

    Application Number : 40794

    Regulatory Info : RX

    Registration Country : USA

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    17

    Teva Pharmaceutical Industries

    Israel
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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 2006-10-27

    Application Number : 40620

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/ML

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    Approval Date : 2006-10-27

    Application Number : 40620

    Regulatory Info : DISCN

    Registration Country : USA

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    HONG KONG

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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

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    Approval Date : 2005-02-23

    Application Number : 40557

    Regulatory Info : RX

    Registration Country : USA

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    HONG KONG

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    Brand Name : METHYLPREDNISOLONE ACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 80MG/ML

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    Approval Date : 2005-02-23

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