01 4BENAZEPRIL HYDROCHLORIDE
02 4BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
03 4BUMETANIDE
04 3CARBAMAZEPINE
05 6DESIPRAMINE HYDROCHLORIDE
06 5DOLASETRON MESYLATE
07 3FUROSEMIDE
08 3HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE
09 2METOPROLOL TARTRATE
10 1PENTOXIFYLLINE
01 3CAPSULE, EXTENDED RELEASE;ORAL
02 4INJECTABLE;INJECTION
03 1TABLET, EXTENDED RELEASE;ORAL
04 27TABLET;ORAL
01 10.25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.5MG
03 4100MG
04 1100MG/5ML (20MG/ML)
05 210MG
06 110MG;12.5MG
07 112.5MG/0.625ML (20MG/ML)
08 1150MG
09 11MG
10 1200MG
11 220MG
12 120MG;12.5MG
13 120MG;25MG
14 125MG
15 125MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 125MG;50MG
17 12MG
18 1300MG
19 1400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 240MG
21 1500MG/25ML (20MG/ML)
22 350MG
23 150MG;100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
24 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 15MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 175MG
27 180MG
01 11DISCN
02 24RX
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN
Dosage Strength : 5MG **Federal Register d...
Approval Date : 1991-06-25
Application Number : 19851
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN
Dosage Strength : 10MG
Approval Date : 1991-06-25
Application Number : 19851
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN
Dosage Strength : 20MG
Approval Date : 1991-06-25
Application Number : 19851
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN
Dosage Strength : 40MG
Approval Date : 1991-06-25
Application Number : 19851
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN HCT
Dosage Strength : 5MG;6.25MG **Federal Reg...
Approval Date : 1992-05-19
Application Number : 20033
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN HCT
Dosage Strength : 10MG;12.5MG
Approval Date : 1992-05-19
Application Number : 20033
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN HCT
Dosage Strength : 20MG;25MG
Approval Date : 1992-05-19
Application Number : 20033
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Dosage Form : TABLET; ORAL
Proprietary Name : LOTENSIN HCT
Dosage Strength : 20MG;12.5MG
Approval Date : 1992-05-19
Application Number : 20033
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMEX
Dosage Strength : 1MG
Approval Date : 1983-02-28
Application Number : 18225
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BUMEX
Dosage Strength : 0.5MG
Approval Date : 1983-02-28
Application Number : 18225
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
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