Home NDC 0169-7113 NDC 0169-7113 - TRETTEN 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 0169-7113
Package NDCs from labels 0169-7113-11
Manufacturer Novo Nordisk | Novo Nordisk A/S
Effective date 2020-06-30
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 0169-7113-11 TRETTEN 3 mL in 1 VIAL, GLASS INJECTION, POWDER, LYOPHILIZED, 1 mL 2500 [iU] in 3mL 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0169-7113 TRETTEN (COAGULATION FACTOR XIII A-SUBUNIT (RECOMBINANT)) KIT [NOVO NORDISK] 8 Unmatched 20200714_8664978e-1814-4930-aca5-97a24455f6df.zip
DailyMed Socrata Ingredients#