FDA.reportPublic FDA data

NDC 73362-207 - Yuviwel

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
73362-207
Package NDCs from labels
73362-207-01
Manufacturer
Ascendis Pharma Endocrinology, Inc.
Effective date
2026-03-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Yuviwel - Ascendis Pharma Endocrinology, Inc.Ascendis Pharma Endocrinology, Inc.2026-03-25HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73362-207-01Yuviwel1 in 1 VIAL, GLASSINJECTION, POWDER, LYOPHILIZED,15.5 mg4