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    Nalbuphine Hydrochloride

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    01 2Rusan Pharma

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    01

    Rusan Pharma

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    Nalbuphine Hydrochloride

    Brand Name :

    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

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

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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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    Nalbuphine Hydrochloride

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    05

    Dr. Reddy's Laboratories

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

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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

    U.S.A
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    ABRAXIS PHARM

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

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    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 : INJECTABLE;INJECTION

    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.

    U.S.A
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    Hospira, Inc.

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    Pharma, Lab & Chemical Expo
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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
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    Hospira, Inc.

    U.S.A
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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
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    Hospira, Inc.

    U.S.A
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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 : 70918

    Regulatory Info : RX

    Registration Country : USA

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    13

    IGI Labs, Inc.

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    IGI Labs, Inc.

    U.S.A
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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
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    Not Confirmed
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    IGI Labs, Inc.

    U.S.A
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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.

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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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
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    IGI Labs, Inc.

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    Pharma, Lab & Chemical Expo
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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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.

    U.S.A
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : DISCN

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    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
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    Quad Pharma

    South Africa
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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
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    Not Confirmed
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    Quad Pharma

    South Africa
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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
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 2019-02-06

    Application Number : 206506

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Rising Pharmaceuticals Inc

    U.S.A
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    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

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    Approval Date : 2019-02-06

    Application Number : 206506

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    23

    Rising Pharmaceuticals Inc

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    Rising Pharmaceuticals Inc

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    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 2019-01-11

    Application Number : 207595

    Regulatory Info : DISCN

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    Rising Pharmaceuticals Inc

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    Rising Pharmaceuticals Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NALBUPHINE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/ML

    Packaging :

    Approval Date : 2019-01-11

    Application Number : 207595

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Somerset Pharmaceuticals Inc

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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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
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • WHO-GMP
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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
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Somerset Pharmaceuticals Inc

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Digital Content Digital Content

    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

    blank

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    29

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : INJECTABLE;INJECTION

    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
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • EDQM
    • WHO-GMP
    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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    Flag Country
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    NALBUPHINE HYDROCHLORIDE

    Brand Name : NUBAIN

    Dosage Form : INJECTABLE;INJECTION

    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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