Home NDC 59572-962 NDC 59572-962 - ISTODAX 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 59572-962
Package NDCs from labels 59572-962-10
Manufacturer Celgene Corporation
Effective date 2023-01-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type ISTODAX - Celgene Corporation Celgene Corporation 2023-01-31 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59572-962-10 ISTODAX 2.2 mL in 1 VIAL, GLASS INJECTION, POWDER, LYOPHILIZED, 2.2 mL 10 mg in 2mL 21
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59572-962 ISTODAX (ROMIDEPSIN) KIT [CELGENE CORPORATION] 21 Unmatched 20230603_03b39d40-90fe-11df-9de6-0002a5d5c51b.zip
DailyMed Socrata Ingredients#