FDA.reportPublic FDA data

NDC 71127-1100 - Sevenfact

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
71127-1100
Package NDCs from labels
71127-1100-1
Manufacturer
Laboratoire Français du Fractionnement et des Biotechnologies Société Anonyme (LFB S.A.)
Effective date
2025-11-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SevenfactLaboratoire Français du Fractionnement et des Biotechnologies Société Anonyme (LFB S.A.)2025-11-19HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71127-1100-1Sevenfact1 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,1 mL1 mg in 1mL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71127-1100SEVENFACT (COAGULATION FACTOR VIIA RECOMBINANT HUMAN) KIT [LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES SOCIÉTÉ ANONYME (LFB S.A.)]9Unmatched20250325_b23ad666-8ce0-4e0b-9eff-c6983ac5f7e6.zip