Home NDC 83457-123 NDC 83457-123 - Humira 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 83457-123
Package NDCs from labels 83457-123-01
Manufacturer Cordavis Limited
Effective date 2025-12-23
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Humira - Cordavis Limited Cordavis Limited 2025-12-23 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83457-123-01 Humira 1 in 1 TRAY INJECTION, SOLUTION 80 mg in 0.8mL 4 83457-123-01 Humira 0.8 mL in 1 SYRINGE INJECTION, SOLUTION 1.6 mL in 2 80 mg in 0.8mL 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83457-123 HUMIRA (ADALIMUMAB) KIT [CORDAVIS LIMITED] 1 Unmatched 20240217_4977567e-3525-44ac-9ff5-f1e74b053950.zip