FDA.reportPublic FDA data

NDC 55292-135 - Signifor LAR

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
55292-135
Package NDCs from labels
55292-135-01
Manufacturer
Recordati Rare Diseases, Inc.
Effective date
2024-07-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Signifor LAR - Recordati Rare Diseases, Inc.Recordati Rare Diseases, Inc.2024-07-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55292-135-01Signifor LAR6 mL in 1 VIAL, SINGLE-USEINJECTION, POWDER, FOR SUSPENSIO6 mL10 mg in 1mL17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55292-135SIGNIFOR LAR (PASIREOTIDE) KIT [RECORDATI RARE DISEASES, INC.]17Unmatched20240719_a0aad470-3f38-af97-e053-2995a90a383a.zip