NDC 63323-925 - Romidepsin

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
63323-925
Package NDCs from labels
63323-925-17
Manufacturer
Fresenius Kabi USA, LLC
Effective date
2026-04-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Romidepsin - Fresenius Kabi USA, LLCFresenius Kabi USA, LLC2026-04-29HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63323-925-17Romidepsin2 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,2 mL10 mg in 2mL9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63323-925ROMIDEPSIN KIT [FRESENIUS KABI USA, LLC]8Unmatched20211124_73a2028d-6735-4cd4-b63d-d072df9927a1.zip