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    Maia Pharmaceuticals

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    01 4BACLOFEN

    02 1BIVALIRUDIN

    03 2BORTEZOMIB

    04 3LEVOTHYROXINE SODIUM

    05 1SINCALIDE

    06 2SODIUM BENZOATE; SODIUM PHENYLACETATE

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    01

    Brand Name : BACLOFEN

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

    U.S.A
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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

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

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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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

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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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 : 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

    U.S.A
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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 : 0.05MG/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
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : ANGIOMAX RTU

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

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

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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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 : LEVOTHYROXINE SODIUM

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

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
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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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    09

    Brand Name : LEVOTHYROXINE SODIUM

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

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AP

    LEVOTHYROXINE SODIUM

    Maia Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : LEVOTHYROXINE SODIUM

    Dosage Strength : 200MCG/VIAL

    Approval Date : 2018-12-21

    Application Number : 208749

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    Brand Name : LEVOTHYROXINE SODIUM

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

    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 : No

    TE Code : AP

    LEVOTHYROXINE SODIUM

    Maia Pharmaceuticals

    Dosage Form : POWDER; INTRAVENOUS

    Proprietary Name : LEVOTHYROXINE SODIUM

    Dosage Strength : 500MCG/VIAL

    Approval Date : 2018-12-21

    Application Number : 208749

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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