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Approved Drug Products containing Paxil listed in the FDA Orange Book. Original Data : FDA Website

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$ API Ref.Price (USD/KG) : 457Xls
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01 17APOTEX

02 1APOTEX INC

03 4AUROBINDO PHARMA

04 3AUROBINDO PHARMA USA

05 3CADILA PHARMS LTD

06 4CHARTWELL RX

07 3CSPC OUYI

08 3EPIC PHARMA LLC

09 4JUBILANT GENERICS

10 3LANNETT CO INC

11 3LUPIN LTD

12 4MYLAN

13 4NORVIUM BIOSCIENCE

14 1NOVITIUM PHARMA

15 4OXFORD PHARMS

16 6PRINSTON INC

17 4ROXANE

18 3SCIECURE PHARMA INC

19 4SUN PHARM INDS INC

20 4TEVA PHARMS

21 4UPSHER SMITH LABS

22 4YILING

23 4ZYDUS PHARMS USA

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PharmaCompass

01

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Approval Date : 1992-12-29

Application Number : 20031

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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02

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 1992-12-29

Application Number : 20031

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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03

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 30MG BASE

Approval Date : 1992-12-29

Application Number : 20031

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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04

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 50MG BASE

Approval Date : 1992-12-29

Application Number : 20031

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 1992-12-29

Application Number : 20031

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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06

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : SUSPENSION;ORAL

Dosage Strength : EQ 10MG BASE/5ML

Approval Date : 1997-06-25

Application Number : 20710

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1998-10-09

Application Number : 20885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1998-10-09

Application Number : 20885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

ASC 2024
Not Confirmed
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 30MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1998-10-09

Application Number : 20885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

ASC 2024
Not Confirmed
arrow
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ASC 2024
Not Confirmed

PAROXETINE HYDROCHLORIDE

Brand Name : PAXIL

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1998-10-09

Application Number : 20885

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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