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01 1AbbVie Inc
02 5Strides Pharma Science
03 1ABHAI LLC
04 3Accord healthcare
05 1Actavis Inc
06 1AiPing Pharmaceutical Inc
07 3Ajanta Pharma Limited
08 3Amneal Pharmaceuticals
09 1Apotex Inc
10 1Avet Pharmaceuticals
11 1Beximco Pharmaceuticals
12 3Bionpharma
13 2Chartwell Pharmaceuticals llc
14 1EG Spa
15 1HIBROW HLTHCARE
16 1Hanlim Pharmaceuticals Inc
17 3Impax Laboratories
18 6Johnson & Johnson Innovative Medicine
19 1LABORATOIRE RIVA INC.
20 2Lannett Company, Inc.
21 1Leading Pharma, LLC
22 1McNeil Consumer Health
23 1Novast Laboratories
24 1Novitium Pharma LLC
25 3Osmotica Pharmaceuticals
26 2PHARM ASSOC
27 3PHARMOBEDIENT
28 1PHARMOBEDIENT CNSLTG
29 6Pharmascience Inc.
30 1Quantum Pharma
31 2Rising Pharmaceuticals Inc
32 3Rubicon Research
33 1SANIS HEALTH INC
34 1Smith & Kenner Pharmaceuticals
35 2Teva Pharmaceutical Industries
36 1Trupharma
37 1USL PHARMA
38 3Unique Biotech Limited
39 4Viatris
40 1West-Coast Pharmaceuticals
41 3Zydus Pharmaceuticals
42 1iPharma
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01 2GEL;TRANSDERMAL
02 2SYRUP
03 7SYRUP;ORAL
04 5TAB
05 9TABLET
06 1TABLET, EXTENDED RELEASE; ORAL
07 33TABLET, EXTENDED RELEASE;ORAL
08 18TABLET;ORAL
09 5Tablet
10 1Tablets
11 1Uncoated Tablet
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01 22DISCN
02 4Generic
03 2Originator
04 3Prescription
05 38RX
06 15Blank
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01 1APO-OXYBUTYNIN
02 2DITROPAN
03 3DITROPAN XL
04 1GELNIQUE
05 1Lyrinel 10 mg
06 1Lyrinel 5 mg
07 2Mylan Oxybutynin 5
08 1OBUTIN
09 1OXYB-5
10 1OXYBUTYN EG
11 1OXYBUTYN HYDROCHLORIDE MYLAN GENERICS
12 1OXYBUTYNIN
13 54OXYBUTYNIN CHLORIDE
14 1Oxybutynin Chloride
15 3Oxybutynin Hydrochloride
16 1Oxyrest
17 6PMS-OXYBUTYNIN
18 1RIVA-OXYBUTYNIN
19 1TEVA-OXYBUTYNIN
20 1Blank
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01 10Canada
02 5India
03 2Italy
04 5South Africa
05 1South Korea
06 61USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : GELNIQUE
Dosage Form : GEL;TRANSDERMAL
Dosage Strength : 10% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-01-27
Application Number : 22204
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1997-10-31
Application Number : 75079
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2020-12-17
Application Number : 208165
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : Oxybutynin Hydrochloride
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Oxybutynin Hydrochloride
Dosage Form : Tablet
Dosage Strength : 2.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Oxybutynin Hydrochloride
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1989-04-19
Application Number : 72485
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1996-07-31
Application Number : 74625
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 1999-01-29
Application Number : 75039
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DITROPAN
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17577
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DITROPAN XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1998-12-16
Application Number : 20897
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DITROPAN XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1998-12-16
Application Number : 20897
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DITROPAN XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-06-22
Application Number : 20897
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 1996-03-29
Application Number : 74520
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DITROPAN
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 18211
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 1997-10-15
Application Number : 74997
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1988-12-08
Application Number : 72296
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1988-11-14
Application Number : 71655
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1988-03-10
Application Number : 70746
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OXYBUTYNIN CHLORIDE
Dosage Form : SYRUP;ORAL
Dosage Strength : 5MG/5ML
Packaging :
Approval Date : 1997-02-12
Application Number : 74868
Regulatory Info : DISCN
Registration Country : USA
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