Home NDC 65628-271 NDC 65628-271 - 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 65628-271
Package NDCs from labels 65628-271-03, 65628-271-05, 65628-271-10
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 65628-271-03 Konvomep 90 mL in 1 BOTTLE SOLUTION 90 mL 84 mg in 1mL 6 65628-271-05 Konvomep 150 mL in 1 BOTTLE SOLUTION 150 mL 84 mg in 1mL 6 65628-271-10 Konvomep 300 mL in 1 BOTTLE SOLUTION 300 mL 84 mg in 1mL 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65628-271 KONVOMEP (OMEPRAZOLE AND SODIUM BICARBONATE) KIT [AZURITY PHARMACEUTICALS, INC.] 5 Unmatched 20241208_688ed6f1-d78a-4006-a682-57021cb38a3e.zip