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

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.

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    Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.

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    ANDA Repository

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    FINISHED DOSAGE FORMULATIONS

    PharmaCompass
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    01 1ACETAMINOPHEN; BUTALBITAL

    02 1CALCITRIOL

    03 3CEFDINIR

    04 2CEFPODOXIME PROXETIL

    05 1CEFTRIAXONE SODIUM

    06 3CEFUROXIME AXETIL

    07 2CEPHALEXIN

    08 3CHLORZOXAZONE

    09 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    10 1FLUOCINOLONE ACETONIDE

    11 3LEVETIRACETAM

    12 1LORATADINE

    13 2METHAZOLAMIDE

    14 2METHYLPHENIDATE HYDROCHLORIDE

    15 6MORPHINE SULFATE

    16 2OMEPRAZOLE; SODIUM BICARBONATE

    17 3POTASSIUM CHLORIDE

    18 4PROPRANOLOL HYDROCHLORIDE

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    01

    Brand Name : BUTALBITAL AND ACETA...

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : BUTALBITAL AND ACETA...

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    • WHO-GMP
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    RLD : No

    TE Code : AA

    ACETAMINOPHEN; BUTALBITAL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL AND ACETAMINO...

    Dosage Strength : 300MG;50MG

    Approval Date : 2016-11-15

    Application Number : 207386

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

    blank

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    02

    Brand Name : CALCITRIOL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : CALCITRIOL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code : AA

    CALCITRIOL

    ANDA Repository

    Dosage Form : SOLUTION; ORAL

    Proprietary Name : CALCITRIOL

    Dosage Strength : 1MCG/ML

    Approval Date : 2023-07-28

    Application Number : 203973

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

    blank

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    03

    Brand Name : CEFDINIR

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    RLD : No

    TE Code : AB

    CEFDINIR

    ANDA Repository

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CEFDINIR

    Dosage Strength : 300MG

    Approval Date : 2007-07-18

    Application Number : 65418

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : CEFDINIR

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Bioprocess International Europe
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    RLD : No

    TE Code : AB

    CEFDINIR

    ANDA Repository

    Dosage Form : FOR SUSPENSION; ORAL

    Proprietary Name : CEFDINIR

    Dosage Strength : 125MG/5ML

    Approval Date : 2007-07-18

    Application Number : 65429

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : CEFDINIR

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Bioprocess International Europe
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    RLD : No

    TE Code : AB

    CEFDINIR

    ANDA Repository

    Dosage Form : FOR SUSPENSION; ORAL

    Proprietary Name : CEFDINIR

    Dosage Strength : 250MG/5ML

    Approval Date : 2007-07-18

    Application Number : 65429

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

    blank

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    06

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AB

    CEFPODOXIME PROXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFPODOXIME PROXETIL

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2007-11-14

    Application Number : 65388

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
    arrow

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    • fda
    • EDQM
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    RLD : No

    TE Code : AB

    CEFPODOXIME PROXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFPODOXIME PROXETIL

    Dosage Strength : EQ 200MG BASE

    Approval Date : 2007-11-14

    Application Number : 65388

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

    blank

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    Market
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    08

    Brand Name : CEFTRIAXONE SODIUM

    U.S.A
    Bioprocess International Europe
    Not Confirmed
    arrow

    Brand Name : CEFTRIAXONE SODIUM

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AP

    CEFTRIAXONE SODIUM

    ANDA Repository

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CEFTRIAXONE SODIUM

    Dosage Strength : EQ 10GM BASE/VIAL

    Approval Date : 2017-01-20

    Application Number : 91117

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

    blank

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    Market
    Place

    09

    Brand Name : CEFUROXIME AXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
    arrow

    Brand Name : CEFUROXIME AXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
    arrow
    • 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 : AB

    CEFUROXIME AXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFUROXIME AXETIL

    Dosage Strength : EQ 125MG BASE

    Approval Date : 2008-02-15

    Application Number : 65359

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    Brand Name : CEFUROXIME AXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
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    Brand Name : CEFUROXIME AXETIL

    U.S.A
    Bioprocess International Europe
    Not Confirmed
    arrow
    • 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 : AB

    CEFUROXIME AXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFUROXIME AXETIL

    Dosage Strength : EQ 250MG BASE

    Approval Date : 2008-02-15

    Application Number : 65359

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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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.