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

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    JMC Corporation KR

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    FINISHED DOSAGE FORMULATIONS

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    01 2CROTAMITON

    02 1GLYCOPYRRONIUM TOSYLATE

    03 7MINOCYCLINE HYDROCHLORIDE

    04 2SULCONAZOLE NITRATE

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    Brand Name : EURAX

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    RLD : Yes

    TE Code :

    CROTAMITON

    JMC Corporation KR

    Dosage Form : CREAM; TOPICAL

    Proprietary Name : EURAX

    Dosage Strength : 10%

    Approval Date : 1982-01-01

    Application Number : 6927

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    02

    Brand Name : EURAX

    South Korea
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    RLD : Yes

    TE Code : AT

    CROTAMITON

    JMC Corporation KR

    Dosage Form : LOTION; TOPICAL

    Proprietary Name : EURAX

    Dosage Strength : 10%

    Approval Date : 1982-01-01

    Application Number : 9112

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AT

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    03

    Brand Name : QBREXZA

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    RLD : Yes

    TE Code :

    GLYCOPYRRONIUM TOSYLATE

    JMC Corporation KR

    Dosage Form : CLOTH; TOPICAL

    Proprietary Name : QBREXZA

    Dosage Strength : EQ 2.4% BASE

    Approval Date : 2018-06-28

    Application Number : 210361

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    Brand Name : XIMINO

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    RLD : No

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : XIMINO

    Dosage Strength : EQ 45MG BASE

    Approval Date : 2012-07-11

    Application Number : 201922

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : XIMINO

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    RLD : No

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : XIMINO

    Dosage Strength : EQ 67.5MG BASE

    Approval Date : 2012-07-11

    Application Number : 201922

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : XIMINO

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    RLD : No

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : XIMINO

    Dosage Strength : EQ 90MG BASE

    Approval Date : 2012-07-11

    Application Number : 201922

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : XIMINO

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    RLD : No

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : XIMINO

    Dosage Strength : EQ 112.5MG BASE

    Approval Date : 2012-07-11

    Application Number : 201922

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    Brand Name : XIMINO

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    RLD : No

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : XIMINO

    Dosage Strength : EQ 135MG BASE

    Approval Date : 2012-07-11

    Application Number : 201922

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : AMZEEQ

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    RLD : Yes

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : AEROSOL, FOAM; TOPICAL

    Proprietary Name : AMZEEQ

    Dosage Strength : EQ 4% BASE

    Approval Date : 2019-10-18

    Application Number : 212379

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    Brand Name : ZILXI

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    RLD : Yes

    TE Code :

    MINOCYCLINE HYDROCHLORIDE

    JMC Corporation KR

    Dosage Form : AEROSOL, FOAM; TOPICAL

    Proprietary Name : ZILXI

    Dosage Strength : EQ 1.5% BASE

    Approval Date : 2020-05-28

    Application Number : 213690

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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