Yohimbine HCl
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2020-12-18
- Label type
- BULK INGREDIENT
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:49:48
Label at a glance#
ProductYohimbine HCl
Active ingredientYOHIMBINE HYDROCHLORIDE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| 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#
Products#
Every source-derived product name is available through these pages.
- Yohimbine HCl
- YOHIMBINE HYDROCHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73309-087 | 73309-087-01, 73309-087-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| YOHIMBINE HYDROCHLORIDE | NB2E1YP49F | ACTIM |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

