Regulatory PathRegulatory requirements compared

Active substance

Glucagon

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
Baqsimi3 mgNasal spray · Nasal use2 Nasal ApplicatorSAR 139.50NCE · PrescriptionEli Lilly and CompanyValid
GLUCAGEN HYPOKIT1 mgPowder and solvent for solution for injection · Subcutaneous use1 VialSAR 86.55Generic · PrescriptionNOVO NORDISKValid
GLUCAGEN powder and solvent for solution for injection1 mgPowder and solvent for solution for injection · Subcutaneous use1 VialSAR 52.55Generic · PrescriptionNOVO NORDISKWithdrawn by MAH · Not Marketed
GLUCAGON 1 MG VIAL+SOLVENT 1ML1 mgPowder for injection · Subcutaneous use1 VialSAR 37.30NCE · PrescriptionEli Lilly and CompanyWithdrawn by MAH · Not Marketed
GLUCAGON 10MG VIAL+SOLVENT10 mgPowder for injection · Subcutaneous use1 VialSAR 311.05NCE · PrescriptionEli Lilly and CompanyWithdrawn by MAH · Not Marketed
Indications — CHI Daman Drug Formulary

ANAPHYLACTIC SHOCK; HYPOGLYCEMIA

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
GLUCAGONEQ 1MG BASE/VIALpowder · intramuscular, intravenousFRESENIUS KABI USAPrescription8 May 2015
GLUCAGONEQ 1MG BASE/VIALpowder · intramuscular, intravenous, subcutaneousFRESENIUS KABI USAPrescription8 May 2015
BAQSIMI3MGpowder · nasalAMPHASTAR PHARMS INCPrescription24 Jul 2019
GVOKE PFS1MG/0.2ML (1MG/0.2ML)solution · subcutaneousXERISPrescription10 Sep 2019
GVOKE HYPOPEN0.5MG/0.1ML (0.5MG/0.1ML); 1MG/0.2ML (1MG/0.2ML)solution · subcutaneousXERISPrescription10 Sep 2019
GVOKE KIT1MG/0.2ML (1MG/0.2ML)solution · subcutaneousXERISPrescription10 Sep 2019
GLUCAGON1MG/VIALinjectable · injectionAMPHASTAR PHARMS INCPrescription28 Dec 2020
GLUCAGON1MG/VIALinjectable · injectionMYLAN LABS LTDPrescription12 Dec 2024
GLUCAGON1MG/VIALinjectable · injectionLUPINPrescription22 Jul 2025
GLUCAGON1MG/VIALinjectable · injectionCIPLAPrescription15 Sep 2025
GLUCAGONEQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 10MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**injectable · injectionLILLYDiscontinued14 Nov 1960
GLUCAGENEQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**powder · intramuscular, intravenousNOVO NORDISKDiscontinued22 Jun 1998
GLUCAGENEQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**powder · intramuscular, intravenous, subcutaneousNOVO NORDISKDiscontinued22 Jun 1998
GLUCAGON1MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**injectable · injectionLILLYDiscontinued11 Sep 1998
GVOKE PFS0.5MG/0.1ML (0.5MG/0.1ML)solution · subcutaneousXERISDiscontinued10 Sep 2019
GVOKE VIALDX1MG/0.2ML (1MG/0.2ML)solution · intravenousXERISDiscontinued10 Sep 2019
GLUCAGONEQ 1MG BASE/VIALinjectable · injectionQUAD PHARMSDiscontinued
GLUCAGONEQ 10MG BASE/VIALinjectable · injectionQUAD PHARMSDiscontinued

EMA European Union — centrally authorised medicines

Baqsimi Amphastar France Pharmaceuticals · Authorised · authorised 16 Dec 2019 · ATC H04AA01

Therapeutic indication (EMA)

Baqsimi is indicated for the treatment of severe hypoglycaemia in adults, adolescents, and children aged 4 years and over with diabetes mellitus.

Ogluo Strongbridge Dublin Limited · Authorised · authorised 11 Feb 2021 · ATC H04AA01

Therapeutic indication (EMA)

Ogluo is indicated for the treatment of severe hypoglycaemia in adults, adolescents, and children aged 2 years and over with diabetes mellitus.

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
BAQSIMI024924153 MG / CONTAINERPOWDER · NASALAMPHASTAR PHARMACEUTICALS, INC.

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACBAQSIMI 3 MG SPRAY$292.98014per EA23 Sep 2026
US NADACBAQSIMI 3 MG SPRAY ONE PACK$292.98014per EA23 Sep 2026
US NADACBAQSIMI 3 MG SPRAY TWO PACK$293.03517per EA23 Sep 2026
US NADACGLUCAGON 1 MG EMERGENCY KIT$154.20337per EA23 Sep 2026
US NADACGLUCAGON 1 MG EMERGENCY KIT$240.40425per EA23 Sep 2026
US NADACGLUCAGON 1 MG VIAL$154.20337per EA23 Sep 2026
US NADACGLUCAGON 1 MG VIAL$240.40425per EA23 Sep 2026
US NADACGVOKE HYPOPEN 1-PK 1 MG/0.2 ML$1603.18226per ML23 Sep 2026
US NADACGVOKE HYPOPEN 2-PK 1 MG/0.2 ML$1596.19346per ML23 Sep 2026
US NADACGVOKE HYPOPEN 2PK 0.5 MG/0.1 ML$3202.32985per ML23 Sep 2026
US NADACGVOKE PFS 1-PK 1 MG/0.2 ML SYR$1600.95652per ML23 Sep 2026
US NADACGVOKE PFS 2-PK 1 MG/0.2 ML SYR$1604.33929per ML23 Sep 2026
NHS Drug TariffGlucagon 1mg powder and solvent for solution for injection vials£11.521 vial1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

WHO WHO Model List of Essential Medicines (2025)

  • 18.6. Medicines for hypoglycaemia · core
    Hypoglycaemia in the context of diabetes
    Parenteral > General injections > unspecified: 1 mg per mL as powder and diluent

Safety signals and safety-related labeling changes

  • US FDA 17 Mar 2025 BAQSIMI — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 14 Mar 2025 GVOKE HYPOPEN — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 14 Mar 2025 GVOKE PFS — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 14 Jul 2022 GLUCAGON — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 11 Mar 2021 GLUCAGEN — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide

All safety entries for glucagon →

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.