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    IMIPENEM; CILASTATIN-1

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    01 1ABEX Pharmaceutica

    02 2ACS DOBFAR SPA

    03 2Actavis Inc

    04 1Antibiotice SA

    05 3Associated Biotech

    06 2Aurobindo Pharma Limited

    07 1Austell Laboratories

    08 1Bernofarm Pharmaceutical Company

    09 2Brooks laboratories Limited

    10 2Fresenius SE & Co. KGaA

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    14 5Hospira, Inc.

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    16 1Jodas Expoim Pvt. Ltd

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    19 9Merck & Co

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    01

    ACS DOBFAR SPA

    Italy
    AACR Annual meeting
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    ACS DOBFAR SPA

    Italy
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    Regulatory Info : RX

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL

    Packaging :

    Approval Date : 2011-12-21

    Application Number : 90577

    Regulatory Info : RX

    Registration Country : USA

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    02

    ACS DOBFAR SPA

    Italy
    AACR Annual meeting
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    ACS DOBFAR SPA

    Italy
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    Regulatory Info : RX

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 2011-12-21

    Application Number : 90577

    Regulatory Info : RX

    Registration Country : USA

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    03

    Actavis Inc

    Ireland
    AACR Annual meeting
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    Ireland
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    Regulatory Info :

    Registration Country : Italy

    Imipenem; Cilastatin

    Brand Name : Imipenem And Cilastatin

    Dosage Form : Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use

    Dosage Strength : 10 VIALS EV 500 mg + 500 mg

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    Approval Date :

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    Regulatory Info :

    Registration Country : Italy

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    04

    Aurobindo Pharma Limited

    India
    AACR Annual meeting
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    India
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    Regulatory Info :

    Registration Country : India

    Imipenem; Cilastatin

    Brand Name :

    Dosage Form : Injection

    Dosage Strength : 250MG; 500MG

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    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : India

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    05

    Aurobindo Pharma Limited

    India
    AACR Annual meeting
    Not Confirmed
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    Aurobindo Pharma Limited

    India
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    Registration Country : Italy

    Imipenem; Cilastatin

    Brand Name : Imecitin

    Dosage Form : Imipenem+Cilastatin+500500 Mg 1 Unit Parenteral Use

    Dosage Strength : 1 vial EV 500 mg + 500 mg

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    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    06

    Hikma Pharmaceuticals

    United Kingdom
    AACR Annual meeting
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    Hikma Pharmaceuticals

    United Kingdom
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    Registration Country : Italy

    Imipenem; Cilastatin

    Brand Name : Imipenem And Cilastatin

    Dosage Form : Imipenem+Cilastatin+500500 Mg 10 Units Parenteral Use

    Dosage Strength : 10 vials soluz Chk 500 mg + 500 mg

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    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    07

    Hospira, Inc.

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL

    Packaging :

    Approval Date : 2011-11-16

    Application Number : 90825

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Hospira, Inc.

    U.S.A
    AACR Annual meeting
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 2011-11-16

    Application Number : 90825

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Hospira, Inc.

    U.S.A
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 2011-11-16

    Application Number : 91007

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    HQ SPCLT PHARMA

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    HQ SPCLT PHARMA

    U.S.A
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 2019-12-12

    Application Number : 207594

    Regulatory Info : RX

    Registration Country : USA

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    11

    Jeil Pharmaceutical Co., Ltd

    South Korea
    AACR Annual meeting
    Not Confirmed
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    Jeil Pharmaceutical Co., Ltd

    South Korea
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    AACR Annual meeting
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    Regulatory Info : Generic

    Registration Country : South Korea

    Cilastatin; Imipenem

    Brand Name :

    Dosage Form : INJECTION;

    Dosage Strength : 0.5MG; 0.5MG

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Korea

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    12

    Jodas Expoim Pvt. Ltd

    India
    AACR Annual meeting
    Not Confirmed
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    Jodas Expoim Pvt. Ltd

    India
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    AACR Annual meeting
    Not Confirmed
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    Regulatory Info : Generic

    Registration Country : India

    Imipenem; Cilastatin

    Brand Name :

    Dosage Form : Powder for Injection

    Dosage Strength : 250MG; 250MG

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : India

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    13

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Merck & Co

    U.S.A
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    AACR Annual meeting
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1985-11-26

    Application Number : 50587

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Merck & Co

    U.S.A
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    AACR Annual meeting
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    Regulatory Info : RX

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 1985-11-26

    Application Number : 50587

    Regulatory Info : RX

    Registration Country : USA

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    15

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    Merck & Co

    U.S.A
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    AACR Annual meeting
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAMUSCULAR

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 1990-12-14

    Application Number : 50630

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Merck & Co

    U.S.A
    AACR Annual meeting
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAMUSCULAR

    Dosage Strength : EQ 750MG BASE/VIAL;750MG/VIAL

    Packaging :

    Approval Date : 1990-12-14

    Application Number : 50630

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Merck & Co

    U.S.A
    AACR Annual meeting
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    Merck & Co

    U.S.A
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    AACR Annual meeting
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    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL

    Packaging :

    Approval Date : 1987-01-08

    Application Number : 62756

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Merck & Co

    U.S.A
    AACR Annual meeting
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    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

    Packaging :

    Approval Date : 1987-01-08

    Application Number : 62756

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    MSD INTL GMBH

    Singapore
    AACR Annual meeting
    Not Confirmed
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    MSD INTL GMBH

    Singapore
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    AACR Annual meeting
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    Regulatory Info : RX

    Registration Country : USA

    CILASTATIN SODIUM; IMIPENEM; RELEBACTAM

    Brand Name : RECARBRIO

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL;250MG/VIAL

    Packaging :

    Approval Date : 2019-07-16

    Application Number : 212819

    Regulatory Info : RX

    Registration Country : USA

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    20

    Myungmoon Pharm. Co., LTD.

    South Korea
    AACR Annual meeting
    Not Confirmed
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    Myungmoon Pharm. Co., LTD.

    South Korea
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    AACR Annual meeting
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    Regulatory Info : Generic

    Registration Country : South Korea

    Imipenem; Cilastatin Sodium

    Brand Name : Tipem

    Dosage Form : INJECTION

    Dosage Strength : 530MG; 532MG

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Korea

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