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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Jai Radhe Sales is your partner for all your sourcing needs.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    xyz-pharma-m-2024-10-07

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    01 1ACETYLCYSTEINE

    02 1CONIVAPTAN HYDROCHLORIDE

    03 3IBUPROFEN

    04 2LACTULOSE

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    Brand Name : ACETADOTE

    U.S.A
    BioFlorida Conference
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    Brand Name : ACETADOTE

    U.S.A
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    BioFlorida Conference
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    Regulatory Info : RX

    Registration Country : USA

    ACETYLCYSTEINE

    CUMBERLAND PHARMS

    Dosage Form : INJECTABLE;INTRAVENOUS

    Brand Name : ACETADOTE

    Dosage Strength : 6GM/30ML (200MG/ML)

    Packaging :

    Approval Date : 2004-01-23

    Application Number : 21539

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : VAPRISOL

    U.S.A
    BioFlorida Conference
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    Brand Name : VAPRISOL

    U.S.A
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    BioFlorida Conference
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    Regulatory Info :

    Registration Country : USA

    CONIVAPTAN HYDROCHLORIDE

    CUMBERLAND PHARMS

    Dosage Form : INJECTABLE; INJECTION

    Brand Name : VAPRISOL

    Dosage Strength : 20MG

    Packaging :

    Approval Date :

    Application Number : 22016

    Regulatory Info :

    Registration Country : USA

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    03

    Brand Name : CALDOLOR

    U.S.A
    BioFlorida Conference
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    Brand Name : CALDOLOR

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    BioFlorida Conference
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    Regulatory Info : DISCN

    Registration Country : USA

    IBUPROFEN

    CUMBERLAND PHARMS

    Dosage Form : SOLUTION;INTRAVENOUS

    Brand Name : CALDOLOR

    Dosage Strength : 400MG/4ML (100MG/ML)

    Packaging :

    Approval Date : 2009-06-11

    Application Number : 22348

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Brand Name : CALDOLOR

    U.S.A
    BioFlorida Conference
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    Brand Name : CALDOLOR

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    BioFlorida Conference
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    Regulatory Info : RX

    Registration Country : USA

    IBUPROFEN

    CUMBERLAND PHARMS

    Dosage Form : SOLUTION;INTRAVENOUS

    Brand Name : CALDOLOR

    Dosage Strength : 800MG/8ML (100MG/ML)

    Packaging :

    Approval Date : 2009-06-11

    Application Number : 22348

    Regulatory Info : RX

    Registration Country : USA

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    05

    Brand Name : CALDOLOR

    U.S.A
    BioFlorida Conference
    Not Confirmed
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    Brand Name : CALDOLOR

    U.S.A
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    BioFlorida Conference
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    Regulatory Info : RX

    Registration Country : USA

    IBUPROFEN

    CUMBERLAND PHARMS

    Dosage Form : SOLUTION;INTRAVENOUS

    Brand Name : CALDOLOR

    Dosage Strength : 800MG/200ML (4MG/ML)

    Packaging :

    Approval Date : 2019-01-25

    Application Number : 22348

    Regulatory Info : RX

    Registration Country : USA

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    06

    Brand Name : LACTULOSE

    U.S.A
    BioFlorida Conference
    Not Confirmed
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    Brand Name : LACTULOSE

    U.S.A
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    BioFlorida Conference
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    Regulatory Info : RX

    Registration Country : USA

    LACTULOSE

    CUMBERLAND PHARMS

    Dosage Form : FOR SOLUTION;ORAL

    Brand Name : LACTULOSE

    Dosage Strength : 10GM/PACKET

    Packaging :

    Approval Date : 1997-12-10

    Application Number : 74712

    Regulatory Info : RX

    Registration Country : USA

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    07

    Brand Name : LACTULOSE

    U.S.A
    BioFlorida Conference
    Not Confirmed
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    Brand Name : LACTULOSE

    U.S.A
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    BioFlorida Conference
    Not Confirmed
    • fda
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    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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    Regulatory Info : RX

    Registration Country : USA

    LACTULOSE

    CUMBERLAND PHARMS

    Dosage Form : FOR SOLUTION;ORAL

    Brand Name : LACTULOSE

    Dosage Strength : 20GM/PACKET

    Packaging :

    Approval Date : 1997-12-10

    Application Number : 74712

    Regulatory Info : RX

    Registration Country : USA

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