Levamisole Hydrochloride
- Manufacturer
- H3 Medical Inc.
- Effective date
- 2019-09-04
- Label type
- BULK INGREDIENT
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:49:21
Label at a glance#
ProductLevamisole Hydrochloride
Active ingredientLEVAMISOLE HYDROCHLORIDE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63732-2048-4 | Levamisole Hydrochloride | 100 g in 1 BOTTLE | POWDER | 100 | 1 | |
| 63732-2048-5 | Levamisole Hydrochloride | 500 g in 1 BOTTLE | POWDER | 500 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63732-2048 | LEVAMISOLE HYDROCHLORIDE POWDER [H3 MEDICAL INC.] | 1 | 2 package rows | 20190905_22a903c0-c30f-4df6-8082-1bc23b68a8c2.zip |
Products#
Every source-derived product name is available through these pages.
- Levamisole Hydrochloride
- LEVAMISOLE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63732-2048 | 63732-2048-4, 63732-2048-5 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LEVAMISOLE HYDROCHLORIDE | DL9055K809 | ACTIB |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
