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    Nephron Pharmaceuticals Corporation

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    01 4ALBUTEROL SULFATE

    02 2ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

    03 2BUDESONIDE

    04 1IPRATROPIUM BROMIDE

    05 1ISOETHARINE HYDROCHLORIDE

    06 1KETOROLAC TROMETHAMINE

    07 2METAPROTERENOL SULFATE

    08 2SODIUM CHLORIDE

    09 1STERILE WATER FOR INJECTION

    10 2VERAPAMIL HYDROCHLORIDE

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    01

    Brand Name : ALBUTEROL SULFATE

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE

    U.S.A
    DCAT Week
    Not Confirmed
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    RLD : No

    TE Code : AN

    ALBUTEROL SULFATE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : ALBUTEROL SULFATE

    Dosage Strength : EQ 0.083% BASE

    Approval Date : 1997-09-17

    Application Number : 74880

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    02

    Brand Name : ALBUTEROL SULFATE

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE

    U.S.A
    DCAT Week
    Not Confirmed
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    RLD : No

    TE Code : AN

    ALBUTEROL SULFATE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : ALBUTEROL SULFATE

    Dosage Strength : EQ 0.5% BASE

    Approval Date : 2001-06-26

    Application Number : 75664

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    03

    Brand Name : ALBUTEROL SULFATE

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE

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    RLD : No

    TE Code : AN

    ALBUTEROL SULFATE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : ALBUTEROL SULFATE

    Dosage Strength : EQ 0.042% BASE

    Approval Date : 2004-06-28

    Application Number : 76355

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    04

    Brand Name : ALBUTEROL SULFATE

    U.S.A
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    Brand Name : ALBUTEROL SULFATE

    U.S.A
    DCAT Week
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    RLD : No

    TE Code : AN

    ALBUTEROL SULFATE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : ALBUTEROL SULFATE

    Dosage Strength : EQ 0.021% BASE

    Approval Date : 2010-03-31

    Application Number : 76355

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    05

    Brand Name : ALBUTEROL SULFATE AN...

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE AN...

    U.S.A
    DCAT Week
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AN

    ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : ALBUTEROL SULFATE AND IP...

    Dosage Strength : EQ 0.083% BASE;0.017%

    Approval Date : 2007-12-31

    Application Number : 76749

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    06

    Brand Name : ALBUTEROL SULFATE; I...

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE; I...

    U.S.A
    DCAT Week
    Not Confirmed
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    RLD :

    TE Code :

    ALBUTEROL SULFATE; IPRATROPIUM BROMIDE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : ALBUTEROL SULFATE; IPRAT...

    Dosage Strength : 0.5MG; 0.017%

    Approval Date :

    Application Number : 76749

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    07

    Brand Name : BUDESONIDE

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : BUDESONIDE

    U.S.A
    DCAT Week
    Not Confirmed
    arrow
    • fda
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    RLD : No

    TE Code : AN

    BUDESONIDE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SUSPENSION; INHALATION

    Proprietary Name : BUDESONIDE

    Dosage Strength : 0.25MG/2ML

    Approval Date : 2009-03-30

    Application Number : 78202

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

    blank

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    08

    Brand Name : BUDESONIDE

    U.S.A
    DCAT Week
    Not Confirmed
    arrow

    Brand Name : BUDESONIDE

    U.S.A
    DCAT Week
    Not Confirmed
    arrow
    • fda
    • EDQM
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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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    RLD : No

    TE Code : AN

    BUDESONIDE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SUSPENSION; INHALATION

    Proprietary Name : BUDESONIDE

    Dosage Strength : 0.5MG/2ML

    Approval Date : 2009-03-30

    Application Number : 78202

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    09

    Brand Name : IPRATROPIUM BROMIDE

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : IPRATROPIUM BROMIDE

    U.S.A
    DCAT Week
    Not Confirmed
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    RLD : No

    TE Code : AN

    IPRATROPIUM BROMIDE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : IPRATROPIUM BROMIDE

    Dosage Strength : 0.02%

    Approval Date : 2001-09-27

    Application Number : 75562

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    10

    Brand Name : BETA-2

    U.S.A
    DCAT Week
    Not Confirmed
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    Brand Name : BETA-2

    U.S.A
    DCAT Week
    Not Confirmed
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    RLD : No

    TE Code :

    ISOETHARINE HYDROCHLORIDE

    Nephron Pharmaceuticals Corporation

    Dosage Form : SOLUTION; INHALATION

    Proprietary Name : BETA-2

    Dosage Strength : 1%

    Approval Date : 1982-01-01

    Application Number : 86711

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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