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 |
---|---|---|---|---|---|
52652-1001 | Epaned | Enalapril Maleate | Kit | Human Prescription Drug | |
52652-2001 | Xatmep | Methotrexate | Solution | Oral | Human Prescription Drug |
52652-3001 | Qbrelis | Lisinopril | Solution | Oral | Human Prescription Drug |
52652-4001 | Epaned | Enalapril Maleate | Solution | Oral | Human Prescription Drug |
52652-5001 | Katerzia | Amlodipine | Suspension | Oral | Human Prescription Drug |
65628-015 | Firvanq | Vancomycin Hydrochloride | Kit | Human Prescription Drug | |
65628-016 | Firvanq | Vancomycin Hydrochloride | Kit | Human Prescription Drug | |
65628-204 | Firvanq | Vancomycin Hydrochloride | Kit | Human Prescription Drug | |
65628-205 | Firvanq | Vancomycin Hydrochloride | Kit | Human Prescription Drug | |
65628-206 | Firvanq | Vancomycin Hydrochloride | Kit | Human Prescription Drug | |
65628-208 | Firvanq | Vancomycin Hydrochloride | Kit | Human Prescription Drug |