Orange Book product · Brand (NDA)
GLUCAGON
GLUCAGON HYDROCHLORIDE
At a glance
Sep 19, 2019
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 19, 2019
6 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
GLUCAGON HYDROCHLORIDE
Strength
EQ 1MG BASE/VIAL
Dosage form
POWDER
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
TE code
Not listed
Application
NDA 201849
Product number
002
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
