NDC 73309-087-01 - Yohimbine HCl

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: 73309-087
Requested NDC: 73309-087-01
Package NDCs from labels: 73309-087-01, 73309-087-02
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2020-12-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Yohimbine HCl - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2020-12-18	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-087-01	Yohimbine HCl	100 g in 1 JAR	POWDER	100		2
73309-087-02	Yohimbine HCl	50 g in 1 JAR	POWDER	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-087	YOHIMBINE HCL POWDER [BLUEBAY SHANDONG CO.,LTD]	2	2 package rows	20201219_cb8a90db-26e2-4c55-8870-edf3adcf6c43.zip

Reported adverse events (FAERS/openFDA)#

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