DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 6DR REDDYS LABS INC
02 4AMNEAL
03 4AMNEAL PHARMS
04 12ANI PHARMS
05 4APOTEX
06 3AUROBINDO PHARMA
07 6AUROBINDO PHARMA LTD
08 4AUROBINDO PHARMA USA
09 10CHARTWELL RX
10 4COREPHARMA
11 4DR REDDYS LABS LTD
12 4GENPHARM
13 6HERITAGE
14 4HERITAGE PHARMA
15 7LUPIN PHARMS
16 4MYLAN PHARMS INC
17 6NORVIUM BIOSCIENCE
18 4PRINSTON INC
19 4RISING
20 10SANDOZ
21 8SUN PHARM INDS LTD
22 4TEVA
23 6TEVA PHARMS
24 8VALIDUS PHARMS
25 4WATSON LABS
26 2WATSON LABS INC
27 4ZYDUS LIFESCIENCES
28 4ZYDUS PHARMS USA INC
01 9CAPSULE; ORAL
02 58CAPSULE;ORAL
03 83TABLET;ORAL
01 48DISCN
02 93RX
03 9Blank
01 52AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
02 5AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
03 4AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE
04 47BENAZEPRIL HYDROCHLORIDE
05 28BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
06 4LOTENSIN
07 4LOTENSIN HCT
08 6LOTREL
01 127No
02 14Yes
03 9Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 2.5MG BASE;10MG
Approval Date : 2010-04-15
Application Number : 77183
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;10MG
Approval Date : 2010-04-15
Application Number : 77183
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;20MG
Approval Date : 2010-04-15
Application Number : 77183
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;20MG
Approval Date : 2010-04-15
Application Number : 77183
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;40MG
Approval Date : 2011-07-05
Application Number : 90149
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code : AB
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;40MG
Approval Date : 2011-07-05
Application Number : 90149
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-06-25
Application Number : 19851
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
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
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
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
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
Dosage Strength : 40MG
Approval Date : 1991-06-25
Application Number : 19851
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
