Home NDC 68982-142 NDC 68982-142 - NUWIQ 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 68982-142
Package NDCs from labels 68982-142-01
Manufacturer Octapharma USA Inc
Effective date 2024-12-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type NUWIQ - Octapharma USA Inc Octapharma USA Inc 2024-12-26 PLASMA DERIVATIVE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68982-142-01 NUWIQ 2.5 mL in 1 VIAL POWDER, FOR SOLUTION 2.5 mL 500 [iU] in 2.5mL 16
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68982-142 NUWIQ (ANTIHEMOPHILIC FACTOR (RECOMBINANT)) KIT [OCTAPHARMA USA INC] 16 Unmatched 20250201_d6cb51f8-3acd-412c-93ec-41a8017dff3e.zip