Home NDC 0169-7829 NDC 0169-7829 - NOVOEIGHT 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 0169-7829
Package NDCs from labels 0169-7829-11
Manufacturer Novo Nordisk
Effective date 2020-07-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type NOVOEIGHT - Novo Nordisk Novo Nordisk 2020-07-31 PLASMA DERIVATIVE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0169-7829-11 NOVOEIGHT 4 mL in 1 VIAL, GLASS INJECTION, POWDER, LYOPHILIZED, 4 mL 62.5 [iU] in 1mL 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0169-7829 NOVOEIGHT (ANTIHEMOPHILIC FACTOR RECOMBINANT) KIT [NOVO NORDISK] 12 Unmatched 20240524_0a19a631-f494-48ac-8cab-7d572bf7b03d.zip
DailyMed Socrata Ingredients#