NDC Labeler Azurity Pharmaceuticals, Inc.

Azurity Pharmaceuticals, Inc. labeler's code is 52652. The labeler has 11 products that have an assigned National Drug Code.

NDC	Proprietary Name	Non-Proprietary Name	Dosage Form	Route Name	Product Type	Status
52652-1001	Epaned	Enalapril Maleate	Kit		Human Prescription Drug	ACTIVE
52652-2001	Xatmep	Methotrexate	Solution	Oral	Human Prescription Drug	ACTIVE
52652-3001	Qbrelis	Lisinopril	Solution	Oral	Human Prescription Drug	ACTIVE
52652-4001	Epaned	Enalapril Maleate	Solution	Oral	Human Prescription Drug	ACTIVE
52652-5001	Katerzia	Amlodipine	Suspension	Oral	Human Prescription Drug	ACTIVE
65628-015	Firvanq	Vancomycin Hydrochloride	Kit		Human Prescription Drug	ACTIVE
65628-016	Firvanq	Vancomycin Hydrochloride	Kit		Human Prescription Drug	ACTIVE
65628-204	Firvanq	Vancomycin Hydrochloride	Kit		Human Prescription Drug	ACTIVE
65628-205	Firvanq	Vancomycin Hydrochloride	Kit		Human Prescription Drug	ACTIVE
65628-206	Firvanq	Vancomycin Hydrochloride	Kit		Human Prescription Drug	ACTIVE
65628-208	Firvanq	Vancomycin Hydrochloride	Kit		Human Prescription Drug	ACTIVE