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    TerSera Therapeutics

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    01 1CETIRIZINE HYDROCHLORIDE

    02 2GOSERELIN (GOSERELIN ACETATE)

    03 2GOSERELIN ACETATE

    04 2MELOXICAM

    05 2ROLAPITANT HYDROCHLORIDE

    06 1TELOTRISTAT ETIPRATE

    07 4ZICONOTIDE ACETATE

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    Brand Name : QUZYTTIR

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    Pharmtech & Ingredients
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    Brand Name : QUZYTTIR

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    Regulatory Info : RX

    Registration Country : USA

    CETIRIZINE HYDROCHLORIDE

    TerSera Therapeutics

    Dosage Form : SOLUTION;INTRAVENOUS

    Brand Name : QUZYTTIR

    Dosage Strength : 10MG/ML (10MG/ML)

    Packaging :

    Approval Date : 2019-10-04

    Application Number : 211415

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : ZOLADEX

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    Brand Name : ZOLADEX

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    Regulatory Info : Prescription

    Registration Country : Canada

    GOSERELIN (GOSERELIN ACETATE)

    TerSera Therapeutics

    Dosage Form : IMPLANT

    Brand Name : ZOLADEX

    Dosage Strength : 3.6MG

    Packaging : ONE DEPOT

    Approval Date :

    Application Number : 2049325

    Regulatory Info : Prescription

    Registration Country : Canada

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    03

    Brand Name : ZOLADEX LA

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    Regulatory Info : Prescription

    Registration Country : Canada

    GOSERELIN (GOSERELIN ACETATE)

    TerSera Therapeutics

    Dosage Form : IMPLANT

    Brand Name : ZOLADEX LA

    Dosage Strength : 10.8MG

    Packaging : ONE DEPOT

    Approval Date :

    Application Number : 2225905

    Regulatory Info : Prescription

    Registration Country : Canada

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    Brand Name : ZOLADEX

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    Regulatory Info : RX

    Registration Country : USA

    GOSERELIN ACETATE

    TerSera Therapeutics

    Dosage Form : IMPLANT;IMPLANTATION

    Brand Name : ZOLADEX

    Dosage Strength : EQ 3.6MG BASE

    Packaging :

    Approval Date : 1989-12-29

    Application Number : 19726

    Regulatory Info : RX

    Registration Country : USA

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    05

    Brand Name : ZOLADEX

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    Regulatory Info : RX

    Registration Country : USA

    GOSERELIN ACETATE

    TerSera Therapeutics

    Dosage Form : IMPLANT;IMPLANTATION

    Brand Name : ZOLADEX

    Dosage Strength : EQ 10.8MG BASE

    Packaging :

    Approval Date : 1996-01-11

    Application Number : 20578

    Regulatory Info : RX

    Registration Country : USA

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    06

    Brand Name : QMIIZ ODT

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    Regulatory Info : DISCN

    Registration Country : USA

    MELOXICAM

    TerSera Therapeutics

    Dosage Form : TABLET, ORALLY DISINTEGR...

    Brand Name : QMIIZ ODT

    Dosage Strength : 7.5MG **Federal Regist...

    Packaging :

    Approval Date : 2018-10-19

    Application Number : 211210

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Brand Name : QMIIZ ODT

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    Regulatory Info : DISCN

    Registration Country : USA

    MELOXICAM

    TerSera Therapeutics

    Dosage Form : TABLET, ORALLY DISINTEGR...

    Brand Name : QMIIZ ODT

    Dosage Strength : 15MG **Federal Registe...

    Packaging :

    Approval Date : 2018-10-19

    Application Number : 211210

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : VARUBI

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    ROLAPITANT HYDROCHLORIDE

    TerSera Therapeutics

    Dosage Form : TABLET;ORAL

    Brand Name : VARUBI

    Dosage Strength : EQ 90MG BASE

    Packaging :

    Approval Date : 2015-09-01

    Application Number : 206500

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : VARUBI

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    Regulatory Info : DISCN

    Registration Country : USA

    ROLAPITANT HYDROCHLORIDE

    TerSera Therapeutics

    Dosage Form : EMULSION;INTRAVENOUS

    Brand Name : VARUBI

    Dosage Strength : EQ 166.5MG BASE/92.5ML...

    Packaging :

    Approval Date : 2017-10-25

    Application Number : 208399

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : XERMELO

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    TELOTRISTAT ETIPRATE

    TerSera Therapeutics

    Dosage Form : TABLET;ORAL

    Brand Name : XERMELO

    Dosage Strength : EQ 250MG BASE

    Packaging :

    Approval Date : 2017-02-28

    Application Number : 208794

    Regulatory Info : RX

    Registration Country : USA

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