FDA.reportPublic FDA data

Yohimbine HCl

Manufacturer
Nanjing Chemlin Biomedical Science & Technology Co, Ltd.
Effective date
2024-08-23
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
2
Source
full-release
Hydrated at
2026-06-01 02:51:08

Label at a glance#

ProductYohimbine HCl
Active ingredientYOHIMBINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Yohimbine HCl

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86036-02286036-022-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
YOHIMBINE HYDROCHLORIDENB2E1YP49FACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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