Home NDC 65628-270 NDC 65628-270 - Konvomep This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 65628-270
Package NDCs from labels 65628-270-03, 65628-270-05, 65628-270-10
Manufacturer Azurity Pharmaceuticals, Inc.
Effective date 2025-12-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65628-270-03 Konvomep 90 mL in 1 BOTTLE SUSPENSION 90 mL 2 mg in 1mL 6 65628-270-05 Konvomep 150 mL in 1 BOTTLE SUSPENSION 150 mL 2 mg in 1mL 6 65628-270-10 Konvomep 300 mL in 1 BOTTLE SUSPENSION 300 mL 2 mg in 1mL 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65628-270 KONVOMEP (OMEPRAZOLE AND SODIUM BICARBONATE) KIT [AZURITY PHARMACEUTICALS, INC.] 5 Unmatched 20241208_688ed6f1-d78a-4006-a682-57021cb38a3e.zip