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    Approved Drug Products of Incyte Corporation listed in the FDA Orange Book. Original Data : FDA Website

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    xyz-pharma-m-2024-09-09

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    Veranova: A CDMO that manages complexity with confidence.

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    xyz-pharma-m-2024-09-09

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    Incyte Corporation

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    01 3PEMIGATINIB

    02 1RETIFANLIMAB-DLWR

    03 6RUXOLITINIB PHOSPHATE

    04 1axatilimab-csfr

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    01

    Brand Name : NIKTIMVO

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : NIKTIMVO

    U.S.A
    BioProcess International
    Not Confirmed
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    RLD :

    TE Code :

    axatilimab-csfr

    Incyte Corporation

    Dosage Form : INJECTABLE; INTRAVENOUS

    Proprietary Name : NIKTIMVO

    Dosage Strength : 50 MG/ML

    Approval Date :

    Application Number : 761411

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    02

    Brand Name : PEMAZYRE

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : PEMAZYRE

    U.S.A
    BioProcess International
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    RLD : Yes

    TE Code :

    PEMIGATINIB

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : PEMAZYRE

    Dosage Strength : 4.5MG

    Approval Date : 2020-04-17

    Application Number : 213736

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : PEMAZYRE

    U.S.A
    BioProcess International
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    Brand Name : PEMAZYRE

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    BioProcess International
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    RLD : Yes

    TE Code :

    PEMIGATINIB

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : PEMAZYRE

    Dosage Strength : 9MG

    Approval Date : 2020-04-17

    Application Number : 213736

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : PEMAZYRE

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : PEMAZYRE

    U.S.A
    BioProcess International
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    RLD : Yes

    TE Code :

    PEMIGATINIB

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : PEMAZYRE

    Dosage Strength : 13.5MG

    Approval Date : 2020-04-17

    Application Number : 213736

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    05

    Brand Name : ZYNYZ

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : ZYNYZ

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    RLD :

    TE Code :

    RETIFANLIMAB-DLWR

    Incyte Corporation

    Dosage Form : INJECTABLE; INTRAVENOUS

    Proprietary Name : ZYNYZ

    Dosage Strength : 500MG/20ML(25MG/ML)

    Approval Date :

    Application Number : 761334

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    06

    Brand Name : JAKAFI

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : JAKAFI

    U.S.A
    BioProcess International
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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : JAKAFI

    Dosage Strength : EQ 5MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    07

    Brand Name : JAKAFI

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : JAKAFI

    U.S.A
    BioProcess International
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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : JAKAFI

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    08

    Brand Name : JAKAFI

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : JAKAFI

    U.S.A
    BioProcess International
    Not Confirmed
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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : JAKAFI

    Dosage Strength : EQ 15MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    09

    Brand Name : JAKAFI

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : JAKAFI

    U.S.A
    BioProcess International
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Incyte Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : JAKAFI

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2011-11-16

    Application Number : 202192

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    10

    Brand Name : OPZELURA

    U.S.A
    BioProcess International
    Not Confirmed
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    Brand Name : OPZELURA

    U.S.A
    BioProcess International
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    RLD : Yes

    TE Code :

    RUXOLITINIB PHOSPHATE

    Incyte Corporation

    Dosage Form : CREAM; TOPICAL

    Proprietary Name : OPZELURA

    Dosage Strength : EQ 1.5% BASE

    Approval Date : 2021-09-21

    Application Number : 215309

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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