
Reset all filters
01 2Eli Lilly
02 2Fresenius Kabi USA
03 6Novo Nordisk
04 2Quad Pharma
05 2Zealand Pharma
Reset all filters
01 2INJECTABLE;INJECTION
02 2Injectable; Injection
03 1KIT
04 2POWDER;INTRAMUSCULAR, INTRAVENOUS
05 2POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
06 1Powder And Solvent For Injectable Solution
07 2Powder and liquid for solution for injection
08 2Solution For Injection
Reset all filters
01 2Approved
02 1Authorized
03 4DISCN
04 2RX
05 1Schedule D
06 4Blank
Reset all filters
01 2GLUCAGEN
02 1GLUCAGEN HYPOKIT
03 6GLUCAGON
04 1Glucagen Hypokit
05 2Glucagon Novo Nordisk
06 2Zegalogue
Reset all filters
01 1Canada
02 2Norway
03 1Spain
04 2Sweden
05 8USA
Regulatory Info : DISCN
Registration Country : USA
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Dosage Strength : EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
Regulatory Info : DISCN
Registration Country : USA
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Dosage Strength : EQ 10MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
Regulatory Info : RX
Registration Country : USA
Brand Name : GLUCAGON
Dosage Form : POWDER;INTRAMUSCULAR, INTRAVENOUS
Dosage Strength : EQ 1MG BASE/VIAL
Packaging :
Approval Date : 2015-05-08
Application Number : 201849
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : GLUCAGON
Dosage Form : POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : EQ 1MG BASE/VIAL
Packaging :
Approval Date : 2019-09-19
Application Number : 201849
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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Dosage Strength : EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info :
Registration Country : Norway
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
Regulatory Info :
Registration Country : Norway
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
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
Regulatory Info : Authorized
Registration Country : Spain
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
Regulatory Info :
Registration Country : USA
Brand Name : GLUCAGON
Dosage Form : Injectable; Injection
Dosage Strength : EQ 1MG BASE/VIAL
Packaging :
Approval Date :
Application Number : 71022
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : GLUCAGON
Dosage Form : Injectable; Injection
Dosage Strength : EQ 10MG BASE/VIAL
Packaging :
Approval Date :
Application Number : 71023
Regulatory Info :
Registration Country : USA
Regulatory Info : Approved
Registration Country : Sweden
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
Regulatory Info : Approved
Registration Country : Sweden
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