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    Glucagon chloride

    ACTIVE PHARMA INGREDIENTS

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    01 2Eli Lilly

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    01

    Eli Lilly

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGON

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12122

    Regulatory Info : DISCN

    Registration Country : USA

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    02

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    Regulatory Info : DISCN

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGON

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12122

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGON

    Dosage Form : POWDER;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : EQ 1MG BASE/VIAL

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    Approval Date : 2015-05-08

    Application Number : 201849

    Regulatory Info : RX

    Registration Country : USA

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    04

    Fresenius Kabi USA

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    Regulatory Info : RX

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGON

    Dosage Form : POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : EQ 1MG BASE/VIAL

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    Approval Date : 2019-09-19

    Application Number : 201849

    Regulatory Info : RX

    Registration Country : USA

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    05

    Novo Nordisk

    Denmark
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    Regulatory Info : DISCN

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGEN

    Dosage Form : POWDER;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1998-06-22

    Application Number : 20918

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Novo Nordisk

    Denmark
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    Regulatory Info : DISCN

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGEN

    Dosage Form : POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    Dosage Strength : EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1998-06-22

    Application Number : 20918

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Novo Nordisk

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    Regulatory Info :

    Registration Country : Norway

    Glucagon hydrochloride

    Brand Name : Glucagon Novo Nordisk

    Dosage Form : Powder and liquid for solution for injection

    Dosage Strength : 1 mg

    Packaging : set

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Norway

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    Novo Nordisk

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    Regulatory Info :

    Registration Country : Norway

    Glucagon hydrochloride

    Brand Name : Glucagon Novo Nordisk

    Dosage Form : Powder and liquid for solution for injection

    Dosage Strength : 1 mg

    Packaging : Vials

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Norway

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    09

    Novo Nordisk

    Denmark
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    Regulatory Info : Schedule D

    Registration Country : Canada

    GLUCAGON (RECOMBINANT DNA ORIGIN) (GLUCAGON HYDROCHLORIDE)

    Brand Name : GLUCAGEN HYPOKIT

    Dosage Form : KIT

    Dosage Strength : 1MG/VIAL

    Packaging : 1ML

    Approval Date :

    Application Number : 2333627

    Regulatory Info : Schedule D

    Registration Country : Canada

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    10

    Novo Nordisk

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    Regulatory Info : Authorized

    Registration Country : Spain

    Glucagon Hydrochloride

    Brand Name : Glucagen Hypokit

    Dosage Form : Powder And Solvent For Injectable Solution

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 1994-01-01

    Application Number : 59327

    Regulatory Info : Authorized

    Registration Country : Spain

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    11

    Quad Pharma

    South Africa
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    Regulatory Info :

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGON

    Dosage Form : Injectable; Injection

    Dosage Strength : EQ 1MG BASE/VIAL

    Packaging :

    Approval Date :

    Application Number : 71022

    Regulatory Info :

    Registration Country : USA

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    12

    Quad Pharma

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    Regulatory Info :

    Registration Country : USA

    GLUCAGON HYDROCHLORIDE

    Brand Name : GLUCAGON

    Dosage Form : Injectable; Injection

    Dosage Strength : EQ 10MG BASE/VIAL

    Packaging :

    Approval Date :

    Application Number : 71023

    Regulatory Info :

    Registration Country : USA

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    13

    Zealand Pharma

    Denmark
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    Regulatory Info : Approved

    Registration Country : Sweden

    Dasiglucagon Hydrochloride

    Brand Name : Zegalogue

    Dosage Form : Solution For Injection

    Dosage Strength : 0.6mg/0.6ml

    Packaging :

    Approval Date : 24/07/2024

    Application Number : 20230626000106

    Regulatory Info : Approved

    Registration Country : Sweden

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    Zealand Pharma

    Denmark
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    Regulatory Info : Approved

    Registration Country : Sweden

    Dasiglucagon Hydrochloride

    Brand Name : Zegalogue

    Dosage Form : Solution For Injection

    Dosage Strength : 0.6mg/0.6ml

    Packaging :

    Approval Date : 24/07/2024

    Application Number : 20230626000113

    Regulatory Info : Approved

    Registration Country : Sweden

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