FDA.reportPublic FDA data

NDC 86036-022 - 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
86036-022
Package NDCs from labels
86036-022-00
Manufacturer
Nanjing Chemlin Biomedical Science & Technology Co, Ltd.
Effective date
2024-08-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Yohimbine HClNanjing Chemlin Biomedical Science & Technology Co, Ltd.2024-08-23BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86036-022-00Yohimbine HCl50 g in 1 JARPOWDER502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86036-022YOHIMBINE HCL POWDER [NANJING CHEMLIN BIOMEDICAL SCIENCE & TECHNOLOGY CO, LTD.]21 package rows20240824_d013d1cb-c902-42ef-9949-296a51670e9a.zip

Reported adverse events (FAERS/openFDA)#

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