NDC 72611-780 - Temsirolimus

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
72611-780
Package NDCs from labels
72611-780-01
Manufacturer
Almaject, Inc.
Effective date
2025-12-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Temsirolimus Injection - Almaject, Inc.Almaject, Inc.2025-12-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72611-780-01Temsirolimus1 mL in 1 VIAL, SINGLE-DOSEINJECTION, SOLUTION, CONCENTRATE1 mL25 mg in 1mL6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72611-780TEMSIROLIMUS (TEMSIROLIMUS INJECTION) KIT [ALMAJECT, INC.]5Unmatched20240412_a1f129ff-c0a4-ede7-ae9c-7a3cfa01fe12.zip