Home NDC 64406-013 NDC 64406-013 - Plegridy 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 64406-013
Package NDCs from labels 64406-013-02
Manufacturer Biogen Inc.
Effective date 2025-10-21
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Plegridy - Biogen Inc. Biogen Inc. 2025-10-21 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64406-013-02 Plegridy 0.5 mL in 1 SYRINGE INJECTION, SOLUTION 1 mL 63 ug in 0.5mL 29
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64406-013 PLEGRIDY (PEGINTERFERON BETA-1A) INJECTION, SOLUTION PLEGRIDY PEN (PEGINTERFERON BETA-1A) INJECTION, SOLUTION PLEGRIDY (PEGINTERFERON BETA-1A) KIT [BIOGEN INC.] 28 Unmatched 20241116_08f0ea03-4e6d-195d-aef4-886e32befa95.zip
DailyMed Socrata Ingredients#