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01 3ACTAVIS ELIZABETH

02 2ALEMBIC

03 3APOTHECON

04 2AUROBINDO PHARMA

05 3CADILA

06 3CHARTWELL RX

07 2DASH PHARMS NATCO

08 3EDENBRIDGE PHARMS

09 3EPIC PHARMA LLC

10 3GLENMARK PHARMS LTD

11 2HARMAN FINOCHEM

12 3IVAX SUB TEVA PHARMS

13 3MYLAN

14 5NOVITIUM PHARMA

15 2PRINSTON INC

16 2RUBICON

17 3TEVA

18 3TEVA BRANDED PHARM

19 2TEVA PHARMS

20 2TEVA WOMENS

21 2TRUPHARMA

22 5UNICHEM

23 3WATSON LABS TEVA

24 2ZYDUS LIFESCIENCES

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PharmaCompass

01

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Brand Name : BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG;6.25MG

Approval Date : 2000-09-25

Application Number : 75469

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Brand Name : BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;6.25MG

Approval Date : 2000-09-25

Application Number : 75469

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Brand Name : BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG;6.25MG

Approval Date : 2000-09-25

Application Number : 75469

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE

Brand Name : ZEBETA

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-07-31

Application Number : 19982

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE

Brand Name : ZEBETA

Dosage Form : TABLET;ORAL

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

Approval Date : 1992-07-31

Application Number : 19982

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Brand Name : ZIAC

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG;6.25MG

Approval Date : 1993-03-26

Application Number : 20186

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Brand Name : ZIAC

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG;6.25MG

Approval Date : 1993-03-26

Application Number : 20186

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

08

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE

Brand Name : ZIAC

Dosage Form : TABLET;ORAL

Dosage Strength : 2.5MG;6.25MG

Approval Date : 1993-03-26

Application Number : 20186

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

09

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE

Brand Name : BISOPROLOL FUMARATE

Dosage Form : TABLET;ORAL

Dosage Strength : 5MG

Approval Date : 2002-10-25

Application Number : 75474

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

blank

10

Pharma, Lab & Chemical Expo
Not Confirmed
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Pharma, Lab & Chemical Expo
Not Confirmed

BISOPROLOL FUMARATE

Brand Name : BISOPROLOL FUMARATE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Approval Date : 2002-10-25

Application Number : 75474

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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