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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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    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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    Alnylam Pharmaceuticals

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    01 1GIVOSIRAN SODIUM

    02 1LUMASIRAN SODIUM

    03 1PATISIRAN SODIUM

    04 1VUTRISIRAN SODIUM

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    01

    Brand Name : GIVLAARI

    U.S.A
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    Brand Name : GIVLAARI

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    RLD : Yes

    TE Code :

    GIVOSIRAN SODIUM

    Alnylam Pharmaceuticals

    Dosage Form : SOLUTION; SUBCUTANEOUS

    Proprietary Name : GIVLAARI

    Dosage Strength : EQ 189MG BASE/ML (EQ 189...

    Approval Date : 2019-11-20

    Application Number : 212194

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : OXLUMO

    U.S.A
    Antibody Engineering
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    Brand Name : OXLUMO

    U.S.A
    Antibody Engineering
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    RLD : Yes

    TE Code :

    LUMASIRAN SODIUM

    Alnylam Pharmaceuticals

    Dosage Form : SOLUTION; SUBCUTANEOUS

    Proprietary Name : OXLUMO

    Dosage Strength : EQ 94.5MG BASE/0.5ML (EQ...

    Approval Date : 2020-11-23

    Application Number : 214103

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : ONPATTRO

    U.S.A
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    Brand Name : ONPATTRO

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    RLD : Yes

    TE Code :

    PATISIRAN SODIUM

    Alnylam Pharmaceuticals

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : ONPATTRO

    Dosage Strength : EQ 10MG BASE/5ML (EQ 2MG...

    Approval Date : 2018-08-10

    Application Number : 210922

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : AMVUTTRA

    U.S.A
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    Brand Name : AMVUTTRA

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    RLD : Yes

    TE Code :

    VUTRISIRAN SODIUM

    Alnylam Pharmaceuticals

    Dosage Form : SOLUTION; SUBCUTANEOUS

    Proprietary Name : AMVUTTRA

    Dosage Strength : EQ 25MG BASE/0.5ML (EQ 2...

    Approval Date : 2022-06-13

    Application Number : 215515

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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