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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Benztropine

    ACTIVE PHARMA INGREDIENTS

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    01 3AIPING PHARM INC

    02 3CHARTWELL RX

    03 3ENDO OPERATIONS

    04 4EPIC PHARMA LLC

    05 1FRESENIUS KABI USA

    06 1HIKMA

    07 1HIKMA FARMACEUTICA

    08 3INVAGEN PHARMS

    09 3LANNETT CO INC

    10 3LEADING

    11 1LUITPOLD

    12 3MERCK

    13 1NAVINTA LLC

    14 3NUVO PHARM

    15 3OXFORD PHARMS

    16 3PLIVA

    17 3QUANTUM PHARMICS

    18 3USL PHARMA

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    01

    AIPING PHARM INC

    U.S.A
    Antibody Engineering
    Not Confirmed
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    AIPING PHARM INC

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code : AA

    BENZTROPINE MESYLATE

    Brand Name : BENZTROPINE MESYLATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Approval Date : 1996-12-12

    Application Number : 40103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    02

    AIPING PHARM INC

    U.S.A
    Antibody Engineering
    Not Confirmed
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    AIPING PHARM INC

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code : AA

    BENZTROPINE MESYLATE

    Brand Name : BENZTROPINE MESYLATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 1996-12-12

    Application Number : 40103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    03

    AIPING PHARM INC

    U.S.A
    Antibody Engineering
    Not Confirmed
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    AIPING PHARM INC

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code : AA

    BENZTROPINE MESYLATE

    Brand Name : BENZTROPINE MESYLATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date : 1996-12-12

    Application Number : 40103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    04

    EPIC PHARMA LLC

    U.S.A
    Antibody Engineering
    Not Confirmed
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    EPIC PHARMA LLC

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : Yes

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : COGENTIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 12015

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    MERCK

    U.S.A
    Antibody Engineering
    Not Confirmed
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    MERCK

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : Yes

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : COGENTIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 9193

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    MERCK

    U.S.A
    Antibody Engineering
    Not Confirmed
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    MERCK

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : Yes

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : COGENTIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 9193

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    07

    MERCK

    U.S.A
    Antibody Engineering
    Not Confirmed
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    MERCK

    U.S.A
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
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    RLD : Yes

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : COGENTIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 9193

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    OXFORD PHARMS

    U.S.A
    Antibody Engineering
    Not Confirmed
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    OXFORD PHARMS

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : BENZTROPINE MESYLATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date : 2008-02-14

    Application Number : 40706

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    OXFORD PHARMS

    U.S.A
    Antibody Engineering
    Not Confirmed
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    OXFORD PHARMS

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • 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.
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    Virtual Booth Virtual Booth
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    RLD : No

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : BENZTROPINE MESYLATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Approval Date : 2008-02-14

    Application Number : 40706

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    OXFORD PHARMS

    U.S.A
    Antibody Engineering
    Not Confirmed
    arrow

    OXFORD PHARMS

    U.S.A
    arrow
    Antibody Engineering
    Not Confirmed
    • 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.
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    BENZTROPINE MESYLATE

    Brand Name : BENZTROPINE MESYLATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 2008-02-14

    Application Number : 40706

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

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    Website

    Corporate PDF