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    Taro Pharmaceutical Industries

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    DESONIDE

    Brand Name : DESONIDE

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    Approval Date : 1992-06-30

    Application Number : 73548

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    Approval Date : 1994-08-03

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    DESONIDE

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    Approval Date : 2014-10-31

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    Alembic Pharmaceuticals Limited

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    DESONIDE

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    Approval Date : 2019-10-23

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    Alembic Pharmaceuticals Limited

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    DESONIDE

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    Approval Date : 2020-08-24

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    Alembic Pharmaceuticals Limited

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    DESONIDE

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    Approval Date : 2022-12-08

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    07

    Almirall

    Spain
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    DESONIDE

    Brand Name : VERDESO

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    Approval Date : 2006-09-19

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    08

    Bayer AG

    Germany
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    ACETIC ACID, GLACIAL; DESONIDE

    Brand Name : TRIDESILON

    Dosage Form : SOLUTION/DROPS;OTIC

    Dosage Strength : 2%;0.05%

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    Approval Date : 1982-01-01

    Application Number : 17914

    Regulatory Info : DISCN

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    09

    Cadila Pharmaceuticals

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    DESONIDE

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    Approval Date : 2019-11-20

    Application Number : 210198

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    10

    Cintex

    India
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    Cintex

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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : GEL;TOPICAL

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    Approval Date : 2020-05-11

    Application Number : 202470

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    Registration Country : USA

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    11

    Cosette Pharma

    U.S.A
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    Cosette Pharma

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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : CREAM;TOPICAL

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    Approval Date : 1992-09-28

    Application Number : 74027

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    12

    Encube Ethicals

    India
    Medlab Asia & Asia Health
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    Encube Ethicals

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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : OINTMENT;TOPICAL

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    Approval Date : 2019-01-30

    Application Number : 210998

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    Registration Country : USA

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    13

    Fougera Pharmaceuticals Inc.

    U.S.A
    Medlab Asia & Asia Health
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    Fougera Pharmaceuticals Inc.

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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Packaging :

    Approval Date : 2001-03-12

    Application Number : 75751

    Regulatory Info : RX

    Registration Country : USA

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    14

    Fougera Pharmaceuticals Inc.

    U.S.A
    Medlab Asia & Asia Health
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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : LOTION;TOPICAL

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    Approval Date : 2002-03-19

    Application Number : 75860

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    15

    Galderma

    Switzerland
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    Registration Country : Italy

    Desonide

    Brand Name : Sterades

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    Dosage Strength : Cream Derm 30 G 0.05 G/ 100 G

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    GALDERMA LABS LP

    U.S.A
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    GALDERMA LABS LP

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    DESONIDE

    Brand Name : DESOWEN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

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    Approval Date : 1984-12-14

    Application Number : 19048

    Regulatory Info : RX

    Registration Country : USA

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    17

    GALDERMA LABS LP

    U.S.A
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    GALDERMA LABS LP

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    DESONIDE

    Brand Name : DESOWEN

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

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    Approval Date : 1988-06-15

    Application Number : 71425

    Regulatory Info : RX

    Registration Country : USA

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    18

    GALDERMA LABS LP

    U.S.A
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    GALDERMA LABS LP

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    DESONIDE

    Brand Name : DESOWEN

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 0.05%

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    Approval Date : 1992-01-24

    Application Number : 72354

    Regulatory Info : RX

    Registration Country : USA

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    19

    Glenmark Pharmaceuticals

    India
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    DESONIDE

    Brand Name : DESONIDE

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    Approval Date : 2017-09-15

    Application Number : 209996

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    Hikma Pharmaceuticals

    United Kingdom
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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : OINTMENT;TOPICAL

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    Approval Date : 2017-03-27

    Application Number : 208836

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Leo Pharma

    Denmark
    Medlab Asia & Asia Health
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    Denmark
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    DESONIDE

    Brand Name : DESONATE

    Dosage Form : GEL;TOPICAL

    Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2006-10-20

    Application Number : 21844

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Padagis

    Israel
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    Padagis

    Israel
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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17010

    Regulatory Info : RX

    Registration Country : USA

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    Padagis

    Israel
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    Israel
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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17426

    Regulatory Info : RX

    Registration Country : USA

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    24

    PAI Pharmaceutical Associates

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    PAI Pharmaceutical Associates

    U.S.A
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    Regulatory Info : DISCN

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    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : LOTION;TOPICAL

    Dosage Strength : 0.05%

    Packaging :

    Approval Date : 2017-09-28

    Application Number : 207855

    Regulatory Info : DISCN

    Registration Country : USA

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    PAI Pharmaceutical Associates

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    PAI Pharmaceutical Associates

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    Regulatory Info : DISCN

    Registration Country : USA

    DESONIDE

    Brand Name : DESONIDE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%

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    Approval Date : 2019-03-12

    Application Number : 212002

    Regulatory Info : DISCN

    Registration Country : USA

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    Registration Country : Italy

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    Brand Name : Prenacid

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    Dosage Strength : Coll 10 Ml 0.25%  

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    Registration Country : Italy

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    Brand Name : Prenacid

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    Dosage Strength : Pom Oftalm 10 G 0.25%  

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    Registration Country : Italy

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    Brand Name : Prenacid

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    Dosage Strength : Ung Oftalm 5 G 0.25%

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    Registration Country : Italy

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    GLENMARK SPECLT

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    Regulatory Info : RX

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    Brand Name : DESONIDE

    Dosage Form : LOTION;TOPICAL

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    Approval Date : 2017-09-26

    Application Number : 209494

    Regulatory Info : RX

    Registration Country : USA

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    Regulatory Info : RX

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    Brand Name : DESONIDE

    Dosage Form : CREAM;TOPICAL

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    Approval Date : 2017-07-24

    Application Number : 209729

    Regulatory Info : RX

    Registration Country : USA

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