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    Nalbuphine Hydrochloride

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    01

    Rusan Pharma

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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

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    Dosage Form : Injection

    Dosage Strength : 10mg/ml

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    02

    AbbVie Inc

    U.S.A
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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1.5MG/ML

    Packaging :

    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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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1998-03-19

    Application Number : 74471

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Rusan Pharma

    India
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    05

    Dr. Reddy's Laboratories

    India
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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1998-03-19

    Application Number : 74471

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Abbott Laboratories

    U.S.A
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    Abbott Laboratories

    U.S.A
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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70917

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    ABRAXIS PHARM

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    ABRAXIS PHARM

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1986-07-02

    Application Number : 70751

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    Registration Country : USA

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    08

    ABRAXIS PHARM

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1986-09-24

    Application Number : 70752

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Hospira, Inc.

    U.S.A
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    Hospira, Inc.

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    Regulatory Info : RX

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70914

    Regulatory Info : RX

    Registration Country : USA

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    10

    Hospira, Inc.

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    Hospira, Inc.

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    Regulatory Info : RX

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70915

    Regulatory Info : RX

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
    BePharma
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    Hospira, Inc.

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    BePharma
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    Regulatory Info : RX

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70916

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    BePharma
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    Hospira, Inc.

    U.S.A
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    BePharma
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    Regulatory Info : RX

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1989-02-03

    Application Number : 70918

    Regulatory Info : RX

    Registration Country : USA

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    13

    IGI Labs, Inc.

    U.S.A
    BePharma
    Not Confirmed
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    IGI Labs, Inc.

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

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1989-04-10

    Application Number : 72070

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    IGI Labs, Inc.

    U.S.A
    BePharma
    Not Confirmed
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    IGI Labs, Inc.

    U.S.A
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    BePharma
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1989-04-10

    Application Number : 72071

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    IGI Labs, Inc.

    U.S.A
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    IGI Labs, Inc.

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    BePharma
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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1989-04-10

    Application Number : 72072

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    IGI Labs, Inc.

    U.S.A
    BePharma
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    IGI Labs, Inc.

    U.S.A
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    BePharma
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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1989-04-10

    Application Number : 72073

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    IGI Labs, Inc.

    U.S.A
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    IGI Labs, Inc.

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 1989-04-10

    Application Number : 72074

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    IGI Labs, Inc.

    U.S.A
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    IGI Labs, Inc.

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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

    Packaging :

    Approval Date : 1989-04-10

    Application Number : 72075

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Quad Pharma

    South Africa
    BePharma
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    Quad Pharma

    South Africa
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    BePharma
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    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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    Quad Pharma

    South Africa
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    Quad Pharma

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    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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    21

    Rising Pharmaceuticals Inc

    U.S.A
    BePharma
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    Rising Pharmaceuticals Inc

    U.S.A
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    BePharma
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    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 2019-02-06

    Application Number : 206506

    Regulatory Info : DISCN

    Registration Country : USA

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    Rising Pharmaceuticals Inc

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    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 20MG/ML

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    Approval Date : 2019-02-06

    Application Number : 206506

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    Rising Pharmaceuticals Inc

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    Rising Pharmaceuticals Inc

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 2019-01-11

    Application Number : 207595

    Regulatory Info : DISCN

    Registration Country : USA

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    Rising Pharmaceuticals Inc

    U.S.A
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    Rising Pharmaceuticals Inc

    U.S.A
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    BePharma
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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

    Packaging :

    Approval Date : 2019-01-11

    Application Number : 207595

    Regulatory Info : DISCN

    Registration Country : USA

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    Somerset Pharmaceuticals Inc

    U.S.A
    BePharma
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    BePharma
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    Regulatory Info : RX

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 2024-09-19

    Application Number : 216049

    Regulatory Info : RX

    Registration Country : USA

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    26

    Somerset Pharmaceuticals Inc

    U.S.A
    BePharma
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    BePharma
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    Regulatory Info : RX

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 2024-09-19

    Application Number : 216049

    Regulatory Info : RX

    Registration Country : USA

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    27

    Somerset Pharmaceuticals Inc

    U.S.A
    BePharma
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    BePharma
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    Regulatory Info : RX

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 2024-09-19

    Application Number : 216050

    Regulatory Info : RX

    Registration Country : USA

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    28

    Somerset Pharmaceuticals Inc

    U.S.A
    BePharma
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    BePharma
    Not Confirmed
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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

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 2024-09-19

    Application Number : 216050

    Regulatory Info : RX

    Registration Country : USA

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    29

    ENDO OPERATIONS

    Country
    BePharma
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    BePharma
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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 **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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    30

    ENDO OPERATIONS

    Country
    BePharma
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    BePharma
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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 **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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