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

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    Maia Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 4BACLOFEN

    02 1BIVALIRUDIN

    03 2BORTEZOMIB

    04 2DAPTOMYCIN

    05 3LEVOTHYROXINE SODIUM

    06 1SINCALIDE

    07 2SODIUM BENZOATE; SODIUM PHENYLACETATE

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    01

    Brand Name : BACLOFEN

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    Brand Name : BACLOFEN

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    RLD : No

    TE Code : AP

    BACLOFEN

    Maia Pharmaceuticals

    Dosage Form : INJECTABLE; INTRATHECAL

    Proprietary Name : BACLOFEN

    Dosage Strength : 0.5MG/ML

    Approval Date : 2019-09-11

    Application Number : 210048

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : BACLOFEN

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    Brand Name : BACLOFEN

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    RLD : No

    TE Code : AP

    BACLOFEN

    Maia Pharmaceuticals

    Dosage Form : INJECTABLE; INTRATHECAL

    Proprietary Name : BACLOFEN

    Dosage Strength : 2MG/ML

    Approval Date : 2019-09-11

    Application Number : 210048

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : BACLOFEN

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    RLD : No

    TE Code : AP

    BACLOFEN

    Maia Pharmaceuticals

    Dosage Form : INJECTABLE; INTRATHECAL

    Proprietary Name : BACLOFEN

    Dosage Strength : 1MG/ML

    Approval Date : 2019-07-30

    Application Number : 210315

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    04

    Brand Name : BACLOFEN

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    RLD : No

    TE Code : AP

    BACLOFEN

    Maia Pharmaceuticals

    Dosage Form : INJECTABLE; INTRATHECAL

    Proprietary Name : BACLOFEN

    Dosage Strength : 0.05MG/ML

    Approval Date : 2021-01-15

    Application Number : 210777

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    05

    Brand Name : ANGIOMAX RTU

    U.S.A
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    Brand Name : ANGIOMAX RTU

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    RLD : Yes

    TE Code :

    BIVALIRUDIN

    Maia Pharmaceuticals

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : ANGIOMAX RTU

    Dosage Strength : 250MG/50ML (5MG/ML)

    Approval Date : 2019-07-25

    Application Number : 211215

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    06

    Brand Name : BORTEZOMIB

    U.S.A
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    Not Confirmed
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    Brand Name : BORTEZOMIB

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    RLD : Yes

    TE Code :

    BORTEZOMIB

    Maia Pharmaceuticals

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : BORTEZOMIB

    Dosage Strength : 3.5MG/3.5ML (1MG/ML)

    Approval Date : 2022-07-27

    Application Number : 215331

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    Brand Name : BORTEZOMIB

    U.S.A
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    RLD : Yes

    TE Code :

    BORTEZOMIB

    Maia Pharmaceuticals

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : BORTEZOMIB

    Dosage Strength : 3.5MG/1.4ML (2.5MG/ML)

    Approval Date : 2022-07-27

    Application Number : 215331

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    Brand Name : DAPTOMYCIN

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Brand Name : DAPTOMYCIN

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    RLD :

    TE Code :

    DAPTOMYCIN

    Maia Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : DAPTOMYCIN

    Dosage Strength : 350MG/VIAL

    Approval Date :

    Application Number : 217630

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    09

    Brand Name : DAPTOMYCIN

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Brand Name : DAPTOMYCIN

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    RLD :

    TE Code :

    DAPTOMYCIN

    Maia Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : DAPTOMYCIN

    Dosage Strength : 500MG/VIAL

    Approval Date :

    Application Number : 217630

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    10

    Brand Name : LEVOTHYROXINE SODIUM

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Brand Name : LEVOTHYROXINE SODIUM

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    RLD : No

    TE Code : AP

    LEVOTHYROXINE SODIUM

    Maia Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : LEVOTHYROXINE SODIUM

    Dosage Strength : 100MCG/VIAL

    Approval Date : 2018-12-21

    Application Number : 208749

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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