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

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01 23Antic-calc Tablet, Film Coated
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08 131Film Coated Tablet
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14 5Oral Drop Solution
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17 1Oral Suspension
18 3Paroxetine 10Mg/Ml 60 Ml Oral Use
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20 15Paroxetine 20Mg 28 Combined Oral Use
21 3Paroxetine 2Mg/Ml 150 Ml Oral Use
22 2Paroxetine 33,1Mg/Ml 18,5Ml Oral Use
23 3SUSPENSION;ORAL
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01 3AG-PAROXETINE TABLETS
02 3APO-PAROXETINE
03 2APX-Paroxetine
04 3AURO-PAROXETINE
05 1Adco-Paroxetine 20 mg
06 1Arapaxel
07 8Arketis
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60 1PAROXETINA THINK
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62 1PAROXETINA ZENTIVA ITALY
63 13PAROXETINE
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65 1PAROXETINE-10
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73 7PMS-PAROXETINE
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148 1Paroxiflex
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150 1Paroxin
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152 1Parxet
153 3Paxetin
154 1Paxil 20
155 2Paxtine
156 1Primoxatine
157 1Pyrantin
158 3RIVA-PAROXETINE
159 1ROXETIN
160 2ROXETIN
161 1SERESTILL
162 1SEREUPIN
163 1SEROXAT
164 1STYLIDEN
165 1Sandoz Paroxetine 20
166 1Serestill
167 2Sereupin
168 1Serodur
169 30Seroxat
170 1Serrapress 20
171 1Serrapress 30
172 1Stiliden
173 3TEVA-PAROXETINE
174 1Texine 20 mg
175 1Titroxatine
176 1Xet 20
177 1Zuria
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06 1Jordan
07 23Malta
08 23Norway
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10 5Portugal
11 22South Africa
12 50Spain
13 74Sweden
14 9Switzerland
15 96USA
16 3United Kingdom
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Paroxetin Zentiva
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 17/01/2005
Application Number : 56962
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Deparoc
Dosage Form : TAB
Dosage Strength : 20mg
Packaging : 28X1mg
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Regulatory Info : Generic
Registration Country : South Africa
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Regulatory Info : Approved
Registration Country : Sweden
Paroxetine Hydrochloride Hemihydrate
Brand Name : Paroxetine Orion
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 21/08/2009
Application Number : 20080703000051
Regulatory Info : Approved
Registration Country : Sweden
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
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Registration Country : India
Brand Name : Paroxetine Hydrochloride
Dosage Form : DC Granules
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Paroxetine Hydrochloride
Dosage Form : Tablet
Dosage Strength : 20MG
Packaging :
Approval Date :
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Registration Country : India
Regulatory Info :
Registration Country : Italy
Brand Name : PAROXETINA THINK
Dosage Form : Tablets
Dosage Strength : 20 mg
Packaging : 28 UNITS 20 MG - ORAL USE
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Registration Country : Italy
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Registration Country : Australia
Brand Name : Aropax
Dosage Form : tablet
Dosage Strength : 20 mg
Packaging : 30
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Registration Country : Australia
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Registration Country : Australia
Brand Name : Aropax
Dosage Form : tablet
Dosage Strength : 20 mg
Packaging : 30
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Registration Country : Australia
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Registration Country : India
Brand Name : Paroxetine Hydrochloride
Dosage Form : DC Granules
Dosage Strength : 20MG
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Registration Country : India
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Paroxetine Pensa
Dosage Form : Film Coated Tablet
Dosage Strength : 20MG
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Approval Date : 2007-06-12
Application Number : 68937
Regulatory Info : Authorized
Registration Country : Spain
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Regulatory Info : RX
Registration Country : USA
Brand Name : PAXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
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Approval Date : 1992-12-29
Application Number : 20031
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : PAXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 1992-12-29
Application Number : 20031
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : PAXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 30MG BASE
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Approval Date : 1992-12-29
Application Number : 20031
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : PAXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1992-12-29
Application Number : 20031
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : PAXIL
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 40MG BASE
Packaging :
Approval Date : 1992-12-29
Application Number : 20031
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Deregistered
Registration Country : Sweden
Paroxetine Hydrochloride (Anhydrous)
Brand Name : Paroxin
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 10/01/2003
Application Number : 20030110000151
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Paroxetine Hydrochloride (Anhydrous)
Brand Name : Paroxistad
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 04/10/2002
Application Number : 20021004000555
Regulatory Info : Deregistered
Registration Country : Sweden

Regulatory Info : Deregistered
Registration Country : Sweden
Paroxetine Hydrochloride (Anhydrous)
Brand Name : Primoxatine
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 23/05/2003
Application Number : 20030523000045
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Paroxetine Hydrochloride (Anhydrous)
Brand Name : Serodur
Dosage Form : Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 21/11/2003
Application Number : 20031121000017
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Paroxetine Hydrochloride (Anhydrous)
Brand Name : Titroxatine
Dosage Form : Film Coated Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 23/05/2003
Application Number : 20030523000052
Regulatory Info : Deregistered
Registration Country : Sweden

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