Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.

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01 1Bayer AG
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25 6Teva Pharmaceutical Industries
26 1VERTICE
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01 1AEROSOL, FOAM;TOPICAL
02 1CRE
03 1CREAM
04 7CREAM;TOPICAL
05 9Cream
06 1Cream, Ointment
07 1Cutaneous Emulsion
08 2GEL;TOPICAL
09 6LOTION;TOPICAL
10 1Lotion
11 1OINTMENT
12 9OINTMENT;TOPICAL
13 3Ointment
14 1SOLUTION/DROPS;OTIC
15 1Salve
16 6Blank
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01 12DISCN
02 3Deregistered
03 6Marketed
04 1Originator
05 2PRESCRIPTION
06 14RX
07 13Blank
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01 6Apolar
02 1DESONATE
03 20DESONIDE
04 3DESOWEN
05 1Desona Cream
06 1Desona Lotion
07 1Locatop
08 2PDP-DESONIDE
09 3Prenacid
10 1Reticus
11 2Sterades
12 3Sterax
13 1TRIDESILON
14 1VERDESO
15 5Blank
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01 2Canada
02 4China
03 1India
04 6Italy
05 6Norway
06 1South Africa
07 2South Korea
08 3Sweden
09 26USA
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
Regulatory Info : DISCN
Registration Country : USA
ACETIC ACID, GLACIAL; DESONIDE
Brand Name : TRIDESILON
Dosage Form : SOLUTION/DROPS;OTIC
Dosage Strength : 2%;0.05%
Packaging :
Approval Date : 1982-01-01
Application Number : 17914
Regulatory Info : DISCN
Registration Country : USA
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Regulatory Info : RX
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1992-09-28
Application Number : 74027
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2002-03-19
Application Number : 75860
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : DESOWEN
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1984-12-14
Application Number : 19048
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESOWEN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1988-06-15
Application Number : 71425
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESOWEN
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1992-01-24
Application Number : 72354
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : VERDESO
Dosage Form : AEROSOL, FOAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2006-09-19
Application Number : 21978
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2017-09-26
Application Number : 209494
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2017-07-24
Application Number : 209729
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2017-09-15
Application Number : 209996
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2017-03-27
Application Number : 208836
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 2006-10-20
Application Number : 21844
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1982-01-01
Application Number : 17010
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : GEL;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2020-05-11
Application Number : 202470
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1992-06-30
Application Number : 73548
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1994-08-03
Application Number : 74254
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : DESONIDE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 2014-10-31
Application Number : 202161
Regulatory Info : RX
Registration Country : USA

Regulatory Info : DISCN
Registration Country : USA
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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