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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 012122

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NDA 012122 describes GLUCAGON, which is a drug marketed by Amphastar Pharms Inc, Cipla, Lilly, Lupin Ltd, Mylan Labs Ltd, and Fresenius Kabi Usa, and is included in seven NDAs. It is available from eight suppliers. Additional details are available on the GLUCAGON profile page.

The generic ingredient in GLUCAGON is glucagon hydrochloride. There are twelve drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the glucagon hydrochloride profile page.

Summary for 012122

Tradename:	GLUCAGON
Applicant:	Lilly
Ingredient:	glucagon hydrochloride
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 1MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	Yes

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 10MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons
Approval Date:	Approved Prior to Jan 1, 1982	TE:		RLD:	Yes

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