GLUCAGEN
GLUCAGON HYDROCHLORIDE
Approval overview GLUCAGEN is listed in Drugs@FDA under application 020918 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient GLUCAGON HYDROCHLORIDE Form and strength POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS - EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor NOVO NORDISK Submission history Latest submission status date: 2021-07-20 00:00:00.
Structured Monograph
Clinical summary
Approval overview GLUCAGEN is listed in Drugs@FDA under application 020918 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient GLUCAGON HYDROCHLORIDE Form and strength POWDER;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS - EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor NOVO NORDISK Submission history Latest submission status date: 2021-07-20 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.