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
52652-1001Epaned Enalapril MaleateKitHuman Prescription Drug
52652-2001Xatmep MethotrexateSolutionOralHuman Prescription Drug
52652-3001Qbrelis LisinoprilSolutionOralHuman Prescription Drug
52652-4001Epaned Enalapril MaleateSolutionOralHuman Prescription Drug
52652-5001Katerzia AmlodipineSuspensionOralHuman Prescription Drug
65628-015Firvanq Vancomycin HydrochlorideKitHuman Prescription Drug
65628-016Firvanq Vancomycin HydrochlorideKitHuman Prescription Drug
65628-204Firvanq Vancomycin HydrochlorideKitHuman Prescription Drug
65628-205Firvanq Vancomycin HydrochlorideKitHuman Prescription Drug
65628-206Firvanq Vancomycin HydrochlorideKitHuman Prescription Drug
65628-208Firvanq Vancomycin HydrochlorideKitHuman Prescription Drug