FDA.reportPublic FDA data

NDC 17156-027 - Ceretec

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
17156-027
Package NDCs from labels
17156-027-01
Manufacturer
Medi-Physics, Inc. dba GE Healthcare | GE Healthcare AS
Effective date
2024-01-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ceretec - Medi-Physics, Inc. dba GE Healthcare | GE Healthcare ASMedi-Physics, Inc. dba GE Healthcare | GE Healthcare AS2024-01-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17156-027-01Ceretec2.5 mL in 1 VIAL, GLASSINJECTION, SOLUTION12.5 mL200 ug in 2mL3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17156-027CERETEC (TECHNETIUM TC-99M EXAMETAZIME AND COBALTOUS CHLORIDE) KIT [MEDI-PHYSICS, INC. DBA GE HEALTHCARE]3Unmatched20240120_d9c291e0-cd0d-43d2-87b4-defefd531942.zip