Home NDC 0026-4821 NDC 0026-4821 - Kovaltry 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 0026-4821
Package NDCs from labels 0026-4821-01, 0026-4821-99
Manufacturer Bayer HealthCare LLC
Effective date 2026-03-02
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 0026-4821-01 Kovaltry 2.5 mL in 1 VIAL, SINGLE-USE INJECTION, POWDER, LYOPHILIZED, 2.5 mL 250 [iU] in 2.5mL 18 0026-4821-99 Kovaltry 2.5 mL in 1 VIAL, SINGLE-USE INJECTION, POWDER, LYOPHILIZED, 2.5 mL 250 [iU] in 2.5mL 18
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0026-4821 KOVALTRY (ANTIHEMOPHILIC FACTOR (RECOMBINANT)) KIT [BAYER HEALTHCARE LLC] 16 Unmatched 20241010_89ba5048-469c-4f08-a173-81b0c6f3004d.zip