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    Approved Drug Products containing Prednisolone listed in the FDA Orange Book. Original Data : FDA Website

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    Prednisolone

    ACTIVE PHARMA INGREDIENTS

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    01 1ALLERGAN

    02 1AUROBINDO PHARMA LTD

    03 1BARR

    04 1BUNDY

    05 1CHARTWELL MOLECULAR

    06 2CHARTWELL RX

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    01

    ALLERGAN

    U.S.A
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    RLD : No

    TE Code :

    CHLORAMPHENICOL; PREDNISOLONE

    Brand Name : CHLOROPTIC-P S.O.P.

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 1%;0.5%

    Approval Date : 1982-01-01

    Application Number : 61188

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Abbvie CB

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    02

    SCHERING

    Germany
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    SCHERING

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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : METI-DERM

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.5%

    Approval Date : 1982-01-01

    Application Number : 10209

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    CHARTWELL RX

    U.S.A
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    RLD : No

    TE Code : AA

    PREDNISOLONE

    Brand Name : PREDNISOLONE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 15MG/5ML

    Approval Date : 1999-05-13

    Application Number : 40323

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    04

    IVAX SUB TEVA PHARMS

    U.S.A
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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : PREDNISOLONE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 15MG/5ML

    Approval Date : 1999-05-28

    Application Number : 40287

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    MERCK

    U.S.A
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    MERCK

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    RLD : No

    TE Code :

    PREDNISOLONE TEBUTATE

    Brand Name : HYDELTRA-TBA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Approval Date : 1982-01-01

    Application Number : 10562

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    PHARMACIA AND UPJOHN

    U.S.A
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    PHARMACIA AND UPJOHN

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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : DELTA-CORTEF

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date : 1982-01-01

    Application Number : 9987

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    PFIZER

    U.S.A
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    PFIZER

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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : STERANE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date : 1982-01-01

    Application Number : 9996

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    TEVA PHARMS

    Israel
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    TEVA PHARMS

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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : PREDNISOLONE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 15MG/5ML

    Approval Date : 2000-01-19

    Application Number : 40322

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    WE PHARMS

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    WE PHARMS

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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : PREDNISOLONE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 15MG/5ML

    Approval Date : 1998-05-28

    Application Number : 40192

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    PHARMOBEDIENT CNSLTG

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    PHARMOBEDIENT CNSLTG

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    RLD : No

    TE Code :

    PREDNISOLONE

    Brand Name : PREDNISOLONE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 15MG/5ML

    Approval Date : 2003-09-10

    Application Number : 40313

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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