01 3ACTAVIS ELIZABETH
02 2ALEMBIC
03 3APOTHECON
04 2AUROBINDO PHARMA
05 3AUROBINDO PHARMA LTD
06 3CADILA
07 3CHARTWELL RX
08 2DASH PHARMS NATCO
09 3EDENBRIDGE PHARMS
10 3EPIC PHARMA LLC
11 3GLENMARK PHARMS LTD
12 2HARMAN FINOCHEM
13 3IVAX SUB TEVA PHARMS
14 3MYLAN
15 5NOVITIUM PHARMA
16 2PRINSTON INC
17 3RUBICON RESEARCH
18 3TEVA
19 5TEVA BRANDED PHARM
20 2TEVA PHARMS
21 2TP ANDA HOLDINGS
22 5UNICHEM
23 2UNIQUE PHARM
24 3WATSON LABS TEVA
25 2ZYDUS LIFESCIENCES
01 72TABLET;ORAL
01 24DISCN
02 45RX
03 3Blank
01 25BISOPROLOL FUMARATE
02 42BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
03 2ZEBETA
04 3ZIAC
01 64No
02 5Yes
03 3Blank
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : No
TE Code :
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 :
RLD : Yes
TE Code :
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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
RLD : Yes
TE Code : AB
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
RLD : No
TE Code : AB
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
RLD : No
TE Code : AB
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
