Active Ingredient: GLUCAGON HYDROCHLORIDE
Proprietary Name: GLUCAGEN
Dosage Form; Route of Administration: POWDER; INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Strength: EQ 1MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N020918
Product Number: 002
Approval Date: Jun 22, 1998
Applicant Holder Full Name: NOVO NORDISK PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
