NDC 73309-015-01 - Vorinostat

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: 73309-015
Requested NDC: 73309-015-01
Package NDCs from labels: 73309-015-01, 73309-015-02
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2020-08-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Vorinostat - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2020-08-17	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-015-01	Vorinostat	500 g in 1 JAR	POWDER	500		2
73309-015-02	Vorinostat	1000 g in 1 JAR	POWDER	1000		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-015	VORINOSTAT POWDER [BLUEBAY SHANDONG CO.,LTD]	2	2 package rows	20200818_bbdbd1ec-dabb-41b8-9aa5-d4ce744c32de.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ZOLINZA	VORINOSTAT	Merck Sharp & Dohme LLC	cd86ee78-2781-468b-930c-3c4677bcc092	2024-11-12	Warnings, Adverse reactions	Exact identifier unii: 58IFB293JI

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.