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    01 2Rusan Pharma

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    04 4ABRAXIS PHARM

    05 1Abbott Laboratories

    06 2Arya Pharma (Pty) Ltd

    07 2Cooper Pharma Limited

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    01

    Rusan Pharma

    India
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    CPhI WW Frankfurt
    Booth #9.2B82
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    Virtual BoothRusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

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    Nalbuphine Hydrochloride

    Brand Name :

    Dosage Form : Injection

    Dosage Strength : 10mg/ml

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    Rusan Pharma

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    02

    AbbVie Inc

    U.S.A
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    CRS
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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1.5MG/ML

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    Approval Date : 1993-03-12

    Application Number : 20200

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Dr. Reddy's Laboratories

    India
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    CPhI Korea
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 100MG/10ML (10MG/ML)

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    Approval Date : 1998-03-19

    Application Number : 74471

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Rusan Pharma

    India
    arrow
    CPhI WW Frankfurt
    Booth #9.2B82
    • fda
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    Virtual BoothRusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

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    Nalbuphine Hydrochloride

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    Dosage Form : Injection

    Dosage Strength : 20mg/ml

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    Registration Country : India

    Rusan Pharma

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    05

    Dr. Reddy's Laboratories

    India
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    CPhI Korea
    Attending
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 200MG/10ML (20MG/ML)

    Packaging :

    Approval Date : 1998-03-19

    Application Number : 74471

    Regulatory Info : DISCN

    Registration Country : USA

    Dr Reddy Company Banner

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    06

    Abbott Laboratories

    U.S.A
    CRS
    Not Confirmed
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    Abbott Laboratories

    U.S.A
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    CRS
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML (20MG/ML)

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70917

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    ABRAXIS PHARM

    U.S.A
    CRS
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    CRS
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML (10MG/ML)

    Packaging :

    Approval Date : 1986-07-02

    Application Number : 70751

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    ABRAXIS PHARM

    U.S.A
    CRS
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    CRS
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 100MG/10ML (10MG/ML)

    Packaging :

    Approval Date : 1986-07-02

    Application Number : 70751

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    ABRAXIS PHARM

    U.S.A
    CRS
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    CRS
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML (20MG/ML)

    Packaging :

    Approval Date : 1986-09-24

    Application Number : 70752

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    ABRAXIS PHARM

    U.S.A
    CRS
    Not Confirmed
    arrow

    ABRAXIS PHARM

    U.S.A
    arrow
    CRS
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 200MG/10ML (20MG/ML)

    Packaging :

    Approval Date : 1986-09-24

    Application Number : 70752

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Endo International

    Ireland
    CRS
    Not Confirmed
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    Endo International

    Ireland
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    CRS
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18024

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Endo International

    Ireland
    CRS
    Not Confirmed
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    Endo International

    Ireland
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    CRS
    Not Confirmed
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    Flag Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

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

    Packaging :

    Approval Date : 1982-05-27

    Application Number : 18024

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Endo International

    Ireland
    CRS
    Not Confirmed
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    Endo International

    Ireland
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    CRS
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 100MG/10ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18024

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Endo International

    Ireland
    CRS
    Not Confirmed
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    Endo International

    Ireland
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    CRS
    Not Confirmed
    • fda
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    Flag Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/2ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18024

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Endo International

    Ireland
    CRS
    Not Confirmed
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    Endo International

    Ireland
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    CRS
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 200MG/10ML (20MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-03-02

    Application Number : 18024

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    CRS
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    CRS
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    Regulatory Info : RX

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML (10MG/ML)

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70914

    Regulatory Info : RX

    Registration Country : USA

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    17

    Hospira, Inc.

    U.S.A
    CRS
    Not Confirmed
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    Hospira, Inc.

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

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 100MG/10ML (10MG/ML)

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70915

    Regulatory Info : RX

    Registration Country : USA

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    18

    Hospira, Inc.

    U.S.A
    CRS
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    CRS
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML (20MG/ML)

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70916

    Regulatory Info : RX

    Registration Country : USA

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    19

    Quad Pharma

    South Africa
    CRS
    Not Confirmed
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    Quad Pharma

    South Africa
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    CRS
    Not Confirmed
    • fda
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    Regulatory Info :

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : Injectable; Injection

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date :

    Application Number : 70692

    Regulatory Info :

    Registration Country : USA

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    20

    Quad Pharma

    South Africa
    CRS
    Not Confirmed
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    Quad Pharma

    South Africa
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    CRS
    Not Confirmed
    • fda
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    Regulatory Info :

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : Injectable; Injection

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date :

    Application Number : 70693

    Regulatory Info :

    Registration Country : USA

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