DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 6Dr. Reddy's Laboratories
02 12Strides Pharma Science
03 3AAIPharma Services Corp.
04 12ANI Pharmaceuticals Inc
05 6Actavis Inc
06 8Amneal Pharmaceuticals
07 4Apotex Inc
08 13Aurobindo Pharma Limited
09 10Avet Pharmaceuticals
10 4Chartwell Pharmaceuticals llc
11 4CorePharma, LLC
12 4Genpharma
13 6NORVIUM BIOSCIENCE
14 3NOVARTIS ANIMAL HEALTH CANADA INC
15 7Pfizer Inc
16 4Prinston
17 4Rising Pharmaceuticals Inc
18 10Sandoz B2B
19 8Sun Pharmaceutical Industries Limited
20 10Teva Pharmaceutical Industries
21 8VALIDUS PHARMS
22 4Viatris
23 4XYZ Pharma
24 1Yangtze River Pharmaceutical Group
25 4Zydus Lifesciences
26 4Zydus Pharmaceuticals
01 9CAPSULE; ORAL
02 58CAPSULE;ORAL
03 6Capsule
04 6TABLET
05 83TABLET;ORAL
06 1Tablet
01 48DISCN
02 6Prescription
03 93RX
04 16Blank
01 52AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
02 5AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
03 4AMLODIPINE MALEATE; BENAZEPRIL HYDROCHLORIDE
04 3BENAZEPRIL
05 47BENAZEPRIL HYDROCHLORIDE
06 28BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
07 3FORTEKOR FLAVOR TABS
08 4LOTENSIN
09 4LOTENSIN HCT
10 6LOTREL
11 7Blank
01 6Canada
02 1China
03 6India
04 150USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 2.5MG BASE;10MG
Packaging :
Approval Date : 2010-04-15
Application Number : 77183
Regulatory Info : RX
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 2.5MG BASE;10MG
Packaging :
Approval Date : 2010-07-29
Application Number : 78381
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;10MG
Packaging :
Approval Date : 2010-04-15
Application Number : 77183
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;20MG
Packaging :
Approval Date : 2010-04-15
Application Number : 77183
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;20MG
Packaging :
Approval Date : 2010-04-15
Application Number : 77183
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;40MG
Packaging :
Approval Date : 2011-07-05
Application Number : 90149
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;40MG
Packaging :
Approval Date : 2011-07-05
Application Number : 90149
Regulatory Info : RX
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;10MG
Packaging :
Approval Date : 2010-07-29
Application Number : 78381
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;20MG
Packaging :
Approval Date : 2010-07-29
Application Number : 78381
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;20MG
Packaging :
Approval Date : 2010-07-29
Application Number : 78381
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;40MG
Packaging :
Approval Date : 2010-07-29
Application Number : 78381
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : DISCN
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;40MG
Packaging :
Approval Date : 2010-07-29
Application Number : 78381
Regulatory Info : DISCN
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Amlodipine Besylate; Benazepril Hydrochloride
Brand Name :
Dosage Form : Capsule
Dosage Strength : 2.5MG; 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Amlodipine Besylate; Benazepril Hydrochloride
Brand Name :
Dosage Form : Capsule
Dosage Strength : 5MG; 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Amlodipine Besylate; Benazepril Hydrochloride
Brand Name :
Dosage Form : Capsule
Dosage Strength : 5MG; 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Amlodipine Besylate; Benazepril Hydrochloride
Brand Name :
Dosage Form : Capsule
Dosage Strength : 5MG; 40MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Amlodipine Besylate; Benazepril Hydrochloride
Brand Name :
Dosage Form : Capsule
Dosage Strength : 10MG; 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Amlodipine Besylate; Benazepril Hydrochloride
Brand Name :
Dosage Form : Capsule
Dosage Strength : 10MG; 40MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : LOTREL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 2.5MG BASE;10MG
Packaging :
Approval Date : 1995-03-03
Application Number : 20364
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : LOTREL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;10MG
Packaging :
Approval Date : 1995-03-03
Application Number : 20364
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : LOTREL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 5MG BASE;20MG
Packaging :
Approval Date : 1995-03-03
Application Number : 20364
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Brand Name : LOTREL
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 10MG BASE;20MG
Packaging :
Approval Date : 2002-06-20
Application Number : 20364
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1991-06-25
Application Number : 19851
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date : 1991-06-25
Application Number : 19851
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date : 1991-06-25
Application Number : 19851
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : LOTENSIN
Dosage Form : TABLET;ORAL
Dosage Strength : 40MG
Packaging :
Approval Date : 1991-06-25
Application Number : 19851
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : LOTENSIN HCT
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1992-05-19
Application Number : 20033
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : LOTENSIN HCT
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;12.5MG
Packaging :
Approval Date : 1992-05-19
Application Number : 20033
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : LOTENSIN HCT
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG;25MG
Packaging :
Approval Date : 1992-05-19
Application Number : 20033
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Brand Name : LOTENSIN HCT
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG;12.5MG
Packaging :
Approval Date : 1992-05-19
Application Number : 20033
Regulatory Info : RX
Registration Country : USA
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