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    01 1ABBVIE

    02 2DR REDDYS

    03 1ABBOTT

    04 2ABRAXIS PHARM

    05 2ENDO OPERATIONS

    06 4HOSPIRA

    07 6IGI LABS INC

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    01

    ABBVIE

    U.S.A
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    RLD : No

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1.5MG/ML

    Approval Date : 1993-03-12

    Application Number : 20200

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    DR REDDYS

    India
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    RLD : No

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Approval Date : 1998-03-19

    Application Number : 74471

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Dr Reddy Company Banner

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    03

    DR REDDYS

    India
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    RLD : No

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Approval Date : 1998-03-19

    Application Number : 74471

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Dr Reddy Company Banner

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    04

    ABRAXIS PHARM

    U.S.A
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    RLD : No

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Approval Date : 1986-07-02

    Application Number : 70751

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    ABRAXIS PHARM

    U.S.A
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    RLD : No

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Approval Date : 1986-09-24

    Application Number : 70752

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    HOSPIRA

    U.S.A
    German Wound Congress
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    RLD : No

    TE Code : AP

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Approval Date : 1989-02-03

    Application Number : 70914

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    QUAD PHARMS

    South Africa
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    RLD :

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : Injectable; Injection

    Dosage Strength : 10MG/ML

    Approval Date :

    Application Number : 70692

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    08

    QUAD PHARMS

    South Africa
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    RLD :

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : Injectable; Injection

    Dosage Strength : 20MG/ML

    Approval Date :

    Application Number : 70693

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    09

    ENDO OPERATIONS

    Country
    German Wound Congress
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    ENDO OPERATIONS

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    RLD : Yes

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 18024

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    10

    ENDO OPERATIONS

    Country
    German Wound Congress
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    RLD : Yes

    TE Code :

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-05-27

    Application Number : 18024

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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