NDC 73309-113 - Procarbazine Hydrochloride

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: 73309-113
Package NDCs from labels: 73309-113-01
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2020-04-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Procarbazine Hydrochloride - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2020-04-09	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-113-01	Procarbazine Hydrochloride	100 g in 1 JAR	POWDER	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-113	PROCARBAZINE HYDROCHLORIDE POWDER [BLUEBAY SHANDONG CO.,LTD]	1	1 package rows	20200410_f359ee61-5b28-4fa7-b6b9-e1c7b028d5eb.zip

Reported adverse events (FAERS/openFDA)#

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