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01 3ACTAVIS ELIZABETH

02 2ALEMBIC

03 3APOTHECON

04 2AUROBINDO PHARMA

05 3AUROBINDO PHARMA LTD

06 3CADILA

07 3CHARTWELL RX

08 3EDENBRIDGE PHARMS

09 3EPIC PHARMA LLC

10 3GLENMARK PHARMS LTD

11 2HARMAN FINOCHEM

12 3IVAX SUB TEVA PHARMS

13 2MICRO LABS

14 3MYLAN

15 2NATCO PHARMA USA

16 5NOVITIUM PHARMA

17 2PRINSTON INC

18 3RUBICON RESEARCH

19 3TEVA

20 5TEVA BRANDED PHARM

21 2TEVA PHARMS

22 2TP ANDA HOLDINGS

23 5UNICHEM

24 5UNIQUE PHARM

25 3WATSON LABS TEVA

26 2ZYDUS LIFESCIENCES

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PharmaCompass

01

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

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08

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

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09

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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

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10

AMWC Asia-TDAC
Not Confirmed
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AMWC Asia-TDAC
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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