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01 1Sanofi

02 1AbbVie Inc

03 5Strides Pharma Science

04 1ABHAI LLC

05 5Accord healthcare

06 1Actavis 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 3Janssen-Cilag

19 6Johnson & Johnson Innovative Medicine

20 1LABORATOIRE RIVA INC.

21 2Lannett Company, Inc.

22 1Leading Pharma, LLC

23 1McNeil Consumer Health

24 1Melisana Consumer Health

25 3NORVIUM BIOSCIENCE

26 2Nicobrand Limited

27 1Novast Laboratories

28 1Novitium Pharma LLC

29 3Osmotica Pharmaceuticals

30 2PHARM ASSOC

31 1PHARMOBEDIENT CNSLTG

32 6Pharmascience Inc.

33 1QUANTUM PHARMICS

34 2Rising Pharmaceuticals Inc

35 3Rubicon Research

36 1SANIS HEALTH INC

37 1Smith & Kenner Pharmaceuticals

38 2Teva Pharmaceutical Industries

39 1Trupharma

40 1USL PHARMA

41 3Unique Biotech Limited

42 1Upsher-Smith Laboratories

43 5Viatris

44 1West-Coast Pharmaceuticals

45 3Zydus Pharmaceuticals

46 1iPharma

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PharmaCompass

01

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Pharmtech & Ingredients
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info :

Registration Country : Sweden

oxibutyninhydroklorid

Brand Name : Ditropan

Dosage Form : TABLET

Dosage Strength : 5 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Sanofi Company Banner

02

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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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Dosage Strength : 10% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

Abbvie Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

OXYBUTYNIN CHLORIDE

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

Strides Pharma Science

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : RX

Registration Country : USA

OXYBUTYNIN CHLORIDE

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

Strides Pharma Science

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Oxybutynin Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Oxybutynin Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 2.5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Oxybutynin Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

08

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

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10

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 2006-11-09

Application Number : 76745

Regulatory Info : DISCN

Registration Country : USA

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11

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2007-05-09

Application Number : 76745

Regulatory Info : DISCN

Registration Country : USA

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12

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2007-05-09

Application Number : 76745

Regulatory Info : DISCN

Registration Country : USA

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13

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

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14

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

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15

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

16

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

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17

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

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18

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : SYRUP;ORAL

Dosage Strength : 5MG/5ML

Packaging :

Approval Date : 2004-12-28

Application Number : 76682

Regulatory Info : DISCN

Registration Country : USA

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19

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

20

PHARM ASSOC

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PHARM ASSOC

U.S.A
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

21

PHARM ASSOC

U.S.A
Pharmtech & Ingredients
Not Confirmed
arrow

PHARM ASSOC

U.S.A
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : SYRUP;ORAL

Dosage Strength : 5MG/5ML

Packaging :

Approval Date : 1998-12-18

Application Number : 75137

Regulatory Info : DISCN

Registration Country : USA

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22

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

23

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

24

USL PHARMA

United Kingdom
Pharmtech & Ingredients
Not Confirmed
arrow

USL PHARMA

United Kingdom
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

25

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
Not Confirmed

Oxybutynin Chloride

Brand Name : Oxybutynin Chloride

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Dosage Strength : 15 MG.

Packaging :

Approval Date :

Application Number : 78293

Regulatory Info :

Registration Country : USA

blank

26

QUANTUM PHARMICS

Country
Pharmtech & Ingredients
Not Confirmed
arrow

QUANTUM PHARMICS

Country
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

27

PHARMOBEDIENT CNSLTG

Country
Pharmtech & Ingredients
Not Confirmed
arrow

PHARMOBEDIENT CNSLTG

Country
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

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

blank

28

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2006-11-09

Application Number : 76644

Regulatory Info : DISCN

Registration Country : USA

blank

29

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 2007-05-10

Application Number : 76644

Regulatory Info : DISCN

Registration Country : USA

blank

30

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

OXYBUTYNIN CHLORIDE

Brand Name : OXYBUTYNIN CHLORIDE

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 5MG

Packaging :

Approval Date : 2006-11-09

Application Number : 76702

Regulatory Info : DISCN

Registration Country : USA

blank