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01 8Pfizer Inc

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PharmaCompass

01

BPI West
Not Confirmed
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BPI West
Not Confirmed

VALDECOXIB

Brand Name : BEXTRA

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2001-11-16

Application Number : 21341

Regulatory Info : DISCN

Registration Country : USA

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02

BPI West
Not Confirmed
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BPI West
Not Confirmed

VALDECOXIB

Brand Name : BEXTRA

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2001-11-16

Application Number : 21341

Regulatory Info : DISCN

Registration Country : USA

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03

BPI West
Not Confirmed
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BPI West
Not Confirmed

Valdecoxib

Brand Name : Bextra

Dosage Form : Film Coated Tablet

Dosage Strength : 10mg

Packaging :

Approval Date : 27-03-2003

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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04

BPI West
Not Confirmed
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BPI West
Not Confirmed

Valdecoxib

Brand Name : Bextra

Dosage Form : Film Coated Tablet

Dosage Strength : 20mg

Packaging :

Approval Date : 27-03-2003

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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05

BPI West
Not Confirmed
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BPI West
Not Confirmed

Valdecoxib

Brand Name : Bextra

Dosage Form : Film Coated Tablet

Dosage Strength : 40mg

Packaging :

Approval Date : 27-03-2003

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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06

BPI West
Not Confirmed
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BPI West
Not Confirmed

Valdecoxib

Brand Name : Valdyn

Dosage Form : Film Coated Tablet

Dosage Strength : 10mg

Packaging :

Approval Date : 27-03-2003

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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07

BPI West
Not Confirmed
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BPI West
Not Confirmed

Valdecoxib

Brand Name : Valdyn

Dosage Form : Film Coated Tablet

Dosage Strength : 20mg

Packaging :

Approval Date : 27-03-2003

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

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08

BPI West
Not Confirmed
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BPI West
Not Confirmed

Valdecoxib

Brand Name : Valdyn

Dosage Form : Film Coated Tablet

Dosage Strength : 40mg

Packaging :

Approval Date : 27-03-2003

Application Number : 2.00E+13

Regulatory Info : Deregistered

Registration Country : Sweden

blank