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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Cilastatin Sodium

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    01 2ACS DOBFAR SPA

    02 1Adcock Ingram

    03 1Antibiotice

    04 1Campus Pharma AB

    05 2ELC Group

    06 3Fresenius Kabi AB Brunna

    07 1HQ SPCLT PHARMA

    08 3Hospira, Inc.

    09 1JW Pharmaceutical Corporation

    10 1Karo Pharma

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    15 9Merck & Co

    16 1Myungmoon Pharm. Co., LTD.

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    01

    ACS DOBFAR SPA

    Italy
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    ACS DOBFAR SPA

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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

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    Approval Date : 2011-12-21

    Application Number : 90577

    Regulatory Info : RX

    Registration Country : USA

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    02

    ACS DOBFAR SPA

    Italy
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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

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    Approval Date : 2011-12-21

    Application Number : 90577

    Regulatory Info : RX

    Registration Country : USA

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    03

    Antibiotice

    Romania
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    Romania
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    Regulatory Info :

    Registration Country : Romania

    Imipenem; Cilastatin Sodium

    Brand Name : IMIPENEM/CILASTATIN Atb®

    Dosage Form : powder for injection/Infusion

    Dosage Strength : 500MG; 500MG

    Packaging : Box x 1 vials, Box x 5 vials, Box x 10 vials

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    Registration Country : Romania

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    04

    ELC Group

    United Kingdom
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Imipenem; Cilastatin Sodium

    Brand Name : Imipenem/Cilastatin Elc

    Dosage Form : Powder For Solution For Infusion

    Dosage Strength : 500MG; 500 MG

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    Approval Date : 23-10-2018

    Application Number : 82046

    Regulatory Info : Cancelled

    Registration Country : Spain

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    05

    ELC Group

    United Kingdom
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Imipenem; Cilastatin Sodium

    Brand Name : Imipenem/Cilastatin Elc

    Dosage Form : Powder For Solution For Infusion

    Dosage Strength : 250MG; 250 MG

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    Approval Date : 23-10-2018

    Application Number : 82045

    Regulatory Info : Cancelled

    Registration Country : Spain

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    06

    Fresenius Kabi AB Brunna

    Sweden
    International Sweetener Colloquium
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    Sweden
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    Regulatory Info : Authorized

    Registration Country : Spain

    Imipenem; Cilastatin Sodium

    Brand Name : Imipenem/Cilastatin Kabi

    Dosage Form : Powder For Solution For Infusion

    Dosage Strength : 500MG; 500 MG

    Packaging :

    Approval Date : 25-03-2010

    Application Number : 71285

    Regulatory Info : Authorized

    Registration Country : Spain

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    07

    Fresenius Kabi AB Brunna

    Sweden
    International Sweetener Colloquium
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    Fresenius Kabi AB Brunna

    Sweden
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Imipenem; Cilastatin Sodium

    Brand Name : Imipenem/Cilastatin Kabi

    Dosage Form : Powder For Solution For Infusion

    Dosage Strength : 250MG; 250 MG

    Packaging :

    Approval Date : 25-03-2010

    Application Number : 71282

    Regulatory Info : Cancelled

    Registration Country : Spain

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    08

    Hospira, Inc.

    U.S.A
    International Sweetener Colloquium
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    International Sweetener Colloquium
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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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    09

    Hospira, Inc.

    U.S.A
    International Sweetener Colloquium
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    U.S.A
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    International Sweetener Colloquium
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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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    10

    Hospira, Inc.

    U.S.A
    International Sweetener Colloquium
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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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    11

    HQ SPCLT PHARMA

    U.S.A
    International Sweetener Colloquium
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    HQ SPCLT PHARMA

    U.S.A
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    International Sweetener Colloquium
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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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    12

    JW Pharmaceutical Corporation

    South Korea
    International Sweetener Colloquium
    Not Confirmed
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    JW Pharmaceutical Corporation

    South Korea
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    International Sweetener Colloquium
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    Regulatory Info : Generic

    Registration Country : South Korea

    Cilastatin Sodium

    Brand Name : Prepenem

    Dosage Form : Injection

    Dosage Strength : 500;500MG

    Packaging : 500mg × 10 Vials

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Korea

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    13

    Merck & Co

    U.S.A
    International Sweetener Colloquium
    Not Confirmed
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    Merck & Co

    U.S.A
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    International Sweetener Colloquium
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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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    Merck & Co

    U.S.A
    International Sweetener Colloquium
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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
    International Sweetener Colloquium
    Not Confirmed
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    Merck & Co

    U.S.A
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    International Sweetener Colloquium
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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
    International Sweetener Colloquium
    Not Confirmed
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    Merck & Co

    U.S.A
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    International Sweetener Colloquium
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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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    Merck & Co

    U.S.A
    International Sweetener Colloquium
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    Merck & Co

    U.S.A
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    International Sweetener Colloquium
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    Regulatory Info : DISCN

    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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    Merck & Co

    U.S.A
    International Sweetener Colloquium
    Not Confirmed
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    Merck & Co

    U.S.A
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    International Sweetener Colloquium
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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
    International Sweetener Colloquium
    Not Confirmed
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    MSD INTL GMBH

    Singapore
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    International Sweetener Colloquium
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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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    Myungmoon Pharm. Co., LTD.

    South Korea
    International Sweetener Colloquium
    Not Confirmed
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    Myungmoon Pharm. Co., LTD.

    South Korea
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    International Sweetener Colloquium
    Not Confirmed
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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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    • 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.