NDC 55566-7502 - Menopur

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
55566-7502
Package NDCs from labels
55566-7502-0
Manufacturer
Ferring Pharmaceuticals Inc.
Effective date
2024-11-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Menopur - Ferring Pharmaceuticals Inc.Ferring Pharmaceuticals Inc.2024-11-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55566-7502-0Menopur1 in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,575 [iU]47

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55566-7502MENOPUR (MENOTROPINS) KIT [FERRING PHARMACEUTICALS INC.]35Unmatched20241127_22c8db95-c3db-1770-8086-31356fbabe35.zip

DailyMed Socrata Ingredients#