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    IMIPENEM; CILASTATIN

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    RELATED EXCIPIENT COMPANIES

    MARKET PLACE

    PATENTS & EXCLUSIVITIES

    REF. STANDARDS & IMPURITIES

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    01 2ACS DOBFAR

    02 3HOSPIRA INC

    03 1HQ SPCLT PHARMA

    04 6MERCK

    05 1MSD MERCK CO

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    01

    ACS DOBFAR

    Italy
    2024 ACI Convention
    Not Confirmed
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    ACS DOBFAR

    Italy
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    2024 ACI Convention
    Not Confirmed
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

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

    Approval Date : 2011-12-21

    Application Number : 90577

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    02

    ACS DOBFAR

    Italy
    2024 ACI Convention
    Not Confirmed
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    ACS DOBFAR

    Italy
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    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AP

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

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

    Approval Date : 2011-12-21

    Application Number : 90577

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    HOSPIRA INC

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    HOSPIRA INC

    U.S.A
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

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

    Approval Date : 2011-11-16

    Application Number : 90825

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    HOSPIRA INC

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    HOSPIRA INC

    U.S.A
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    2024 ACI Convention
    Not Confirmed
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : IMIPENEM AND CILASTATIN

    Dosage Form : POWDER;INTRAVENOUS

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

    Approval Date : 2011-11-16

    Application Number : 90825

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    05

    MERCK

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    MERCK

    U.S.A
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    2024 ACI Convention
    Not Confirmed
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    RLD : Yes

    TE Code :

    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**

    Approval Date : 1985-11-26

    Application Number : 50587

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    MERCK

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    MERCK

    U.S.A
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    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
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    RLD : Yes

    TE Code : AP

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAVENOUS

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

    Approval Date : 1985-11-26

    Application Number : 50587

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    07

    MERCK

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    MERCK

    U.S.A
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    2024 ACI Convention
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    • EDQM
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAMUSCULAR

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

    Approval Date : 1990-12-14

    Application Number : 50630

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    MERCK

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    MERCK

    U.S.A
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    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : POWDER;INTRAMUSCULAR

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

    Approval Date : 1990-12-14

    Application Number : 50630

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    MERCK

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    MERCK

    U.S.A
    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : INJECTABLE;INJECTION

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

    Approval Date : 1987-01-08

    Application Number : 62756

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    10

    MERCK

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    MERCK

    U.S.A
    arrow
    2024 ACI Convention
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : No

    TE Code :

    CILASTATIN SODIUM; IMIPENEM

    Brand Name : PRIMAXIN

    Dosage Form : INJECTABLE;INJECTION

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

    Approval Date : 1987-01-08

    Application Number : 62756

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF