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01 7ACCORD HLTHCARE

02 5ACTAVIS ELIZABETH

03 5ALEMBIC

04 7ALEMBIC LTD

05 6AUROBINDO PHARMA USA

06 12CHARTWELL RX

07 7COSETTE

08 5DR REDDYS LABS LTD

09 5ELITE LABS INC

10 7EPIC PHARMA LLC

11 13GLAXOSMITHKLINE LLC

12 7GLENMARK PHARMS LTD

13 7HIKMA

14 7MLV

15 7ORBION PHARMS

16 7PHARMOBEDIENT

17 12PRINSTON INC

18 5SANDOZ INC

19 5WATSON LABS INC

20 7ZYDUS LIFESCIENCES

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PharmaCompass

01

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 0.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-09-19

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-09-19

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

CTAD25
Not Confirmed
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arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-09-19

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

CTAD25
Not Confirmed
arrow
arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-09-19

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

CTAD25
Not Confirmed
arrow
arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1997-09-19

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

06

CTAD25
Not Confirmed
arrow
arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1999-01-27

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

CTAD25
Not Confirmed
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arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1999-01-27

Application Number : 20658

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

CTAD25
Not Confirmed
arrow
arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2008-06-13

Application Number : 22008

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

CTAD25
Not Confirmed
arrow
arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2008-06-13

Application Number : 22008

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

10

CTAD25
Not Confirmed
arrow
arrow
CTAD25
Not Confirmed

ROPINIROLE HYDROCHLORIDE

Brand Name : REQUIP XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 2008-06-13

Application Number : 22008

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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