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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Jai Radhe Sales is your partner for all your sourcing needs.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    01 4BENAZEPRIL HYDROCHLORIDE

    02 4BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    03 4BUMETANIDE

    04 3CARBAMAZEPINE

    05 6DESIPRAMINE HYDROCHLORIDE

    06 5DOLASETRON MESYLATE

    07 3FUROSEMIDE

    08 3HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE

    09 1ISOCARBOXAZID

    10 2METOPROLOL TARTRATE

    11 1PENTOXIFYLLINE

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    01

    Brand Name : LOTENSIN

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : LOTENSIN

    U.S.A
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    RLD : Yes

    TE Code :

    BENAZEPRIL HYDROCHLORIDE

    VALIDUS PHARMS

    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 :

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    02

    Brand Name : LOTENSIN

    U.S.A
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    Brand Name : LOTENSIN

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    RLD : Yes

    TE Code : AB

    BENAZEPRIL HYDROCHLORIDE

    VALIDUS PHARMS

    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

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    03

    Brand Name : LOTENSIN

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    Brand Name : LOTENSIN

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    RLD : Yes

    TE Code : AB

    BENAZEPRIL HYDROCHLORIDE

    VALIDUS PHARMS

    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

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    04

    Brand Name : LOTENSIN

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    Brand Name : LOTENSIN

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    RLD : Yes

    TE Code : AB

    BENAZEPRIL HYDROCHLORIDE

    VALIDUS PHARMS

    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

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    05

    Brand Name : LOTENSIN HCT

    U.S.A
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    Brand Name : LOTENSIN HCT

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    RLD : Yes

    TE Code :

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    VALIDUS PHARMS

    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 :

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    06

    Brand Name : LOTENSIN HCT

    U.S.A
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    Brand Name : LOTENSIN HCT

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    RLD : Yes

    TE Code : AB

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    VALIDUS PHARMS

    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

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    07

    Brand Name : LOTENSIN HCT

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : LOTENSIN HCT

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
    • EDQM
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code : AB

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    VALIDUS PHARMS

    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

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    08

    Brand Name : LOTENSIN HCT

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : LOTENSIN HCT

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
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    RLD : Yes

    TE Code : AB

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    VALIDUS PHARMS

    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

    blank

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    09

    Brand Name : BUMEX

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUMEX

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code : AB

    BUMETANIDE

    VALIDUS PHARMS

    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

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    10

    Brand Name : BUMEX

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUMEX

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code : AB

    BUMETANIDE

    VALIDUS PHARMS

    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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