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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
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE

    U.S.A
    Pharmtech & Ingredients
    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
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE

    U.S.A
    Pharmtech & Ingredients
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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
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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

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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 0.021% 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...

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    Brand Name : ALBUTEROL SULFATE AN...

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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
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    Not Confirmed
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    Brand Name : ALBUTEROL SULFATE; I...

    U.S.A
    Pharmtech & Ingredients
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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
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUDESONIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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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

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    08

    Brand Name : BUDESONIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BUDESONIDE

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
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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
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : IPRATROPIUM BROMIDE

    U.S.A
    Pharmtech & Ingredients
    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
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : BETA-2

    U.S.A
    Pharmtech & Ingredients
    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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