01 4ACCORD HLTHCARE
02 4ACTAVIS ELIZABETH
03 4APOTEX
04 4AUROBINDO PHARMA LTD
05 4CHARTWELL MOLECULAR
06 4CHARTWELL RX
07 4CIPLA
08 4COREPHARMA
09 4HIKMA
10 4KING PFIZER
11 4KING PHARMS LLC
12 4LUPIN
13 4NATCO PHARMA
14 2RANBAXY LABS LTD
15 1ROSEMONT PHARMACEUTICALS INC
16 4SENORES PHARMS
17 4TEVA PHARMS
18 4WATSON LABS
19 4ZYDUS PHARMS USA
20 4ZYDUS PHARMS USA INC
01 58CAPSULE;ORAL
02 1SOLUTION;ORAL
03 16TABLET;ORAL
01 39DISCN
02 35RX
03 1Blank
01 8ALTACE
02 66RAMIPRIL
03 1VOSTALLY
01 66No
02 8Yes
03 1Blank
RLD : No
TE Code : AB
Brand Name : RAMIPRIL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 1.25MG
Approval Date : 2005-10-24
Application Number : 76549
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : RAMIPRIL
Dosage Form : CAPSULE;ORAL
Dosage Strength : 2.5MG
Approval Date : 2005-10-24
Application Number : 76549
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : ALTACE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 1.25MG
Approval Date : 1991-01-28
Application Number : 19901
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : ALTACE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 2.5MG
Approval Date : 1991-01-28
Application Number : 19901
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : ALTACE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 5MG
Approval Date : 1991-01-28
Application Number : 19901
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : ALTACE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 10MG
Approval Date : 1991-01-28
Application Number : 19901
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ALTACE
Dosage Form : TABLET;ORAL
Dosage Strength : 1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2007-02-27
Application Number : 22021
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ALTACE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2007-02-27
Application Number : 22021
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ALTACE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2007-02-27
Application Number : 22021
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ALTACE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2007-02-27
Application Number : 22021
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
