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    Dr. Reddy's Laboratories

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    AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

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    Dr. Reddy's Laboratories

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    Dr. Reddy's Laboratories

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    AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

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    Dr. Reddy's Laboratories

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    Dosage Strength : EQ 10MG BASE;20MG

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    Dr. Reddy's Laboratories

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    AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

    Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 5MG BASE;40MG

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    Approval Date : 2011-07-05

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    Dr. Reddy's Laboratories

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    AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

    Brand Name : AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10MG BASE;40MG

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    Approval Date : 2011-07-05

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    AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

    Brand Name : LOTREL

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    Approval Date : 1995-03-03

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    Brand Name : LOTREL

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    Brand Name : LOTREL

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    Approval Date : 1995-03-03

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    10

    Sandoz B2B

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    Brand Name : LOTREL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10MG BASE;20MG

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    Approval Date : 2002-06-20

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    Sandoz B2B

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    Brand Name : LOTREL

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    Approval Date : 2006-04-11

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    Sandoz B2B

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    Brand Name : LOTREL

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    Approval Date : 2006-04-11

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    13

    VALIDUS PHARMS

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    BENAZEPRIL HYDROCHLORIDE

    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**

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    Approval Date : 1991-06-25

    Application Number : 19851

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    Brand Name : LOTENSIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1991-06-25

    Application Number : 19851

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    BENAZEPRIL HYDROCHLORIDE

    Brand Name : LOTENSIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

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    Approval Date : 1991-06-25

    Application Number : 19851

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    BENAZEPRIL HYDROCHLORIDE

    Brand Name : LOTENSIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

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    Approval Date : 1991-06-25

    Application Number : 19851

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    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**

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    Approval Date : 1992-05-19

    Application Number : 20033

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    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;12.5MG

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    Approval Date : 1992-05-19

    Application Number : 20033

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    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;25MG

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    Approval Date : 1992-05-19

    Application Number : 20033

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    VALIDUS PHARMS

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    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;12.5MG

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    Approval Date : 1992-05-19

    Application Number : 20033

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