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    TerSera Therapeutics

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    01 1GOSERELIN

    02 2GOSERELIN (GOSERELIN ACETATE)

    03 2GOSERELIN ACETATE

    04 2MELOXICAM

    05 2ROLAPITANT HYDROCHLORIDE

    06 1TELOTRISTAT ETIPRATE

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    01

    Brand Name : ZOLADEX

    U.S.A
    PEGS Boston Summit
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    Regulatory Info :

    Registration Country : USA

    GOSERELIN

    TerSera Therapeutics

    Dosage Form : IMPLANT;IMPLANTATION

    Brand Name : ZOLADEX

    Dosage Strength : 3.6MG

    Packaging :

    Approval Date :

    Application Number : 20515

    Regulatory Info :

    Registration Country : USA

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    02

    Brand Name : ZOLADEX

    U.S.A
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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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    04

    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

    U.S.A
    PEGS Boston Summit
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    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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    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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    08

    Brand Name : VARUBI

    U.S.A
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    Brand Name : VARUBI

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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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    09

    Brand Name : VARUBI

    U.S.A
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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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    10

    Brand Name : XERMELO

    U.S.A
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    Brand Name : XERMELO

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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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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.