Toltrazuril
- Manufacturer
- DARMERICA, LLC
- Effective date
- 2026-04-02
- Label type
- BULK INGREDIENT - ANIMAL DRUG
- Version
- 9
- Source
- full-release
- Hydrated at
- 2026-06-01 02:52:44
Label at a glance#
ProductToltrazuril
Active ingredientToltrazuril
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71052-064-05 | Toltrazuril | 5 kg in 1 PACKAGE | POWDER | 5 | 9 | |
| 71052-064-20 | Toltrazuril | 1 kg in 1 PACKAGE | POWDER | 1 | 9 | |
| 71052-064-21 | Toltrazuril | 20 kg in 1 PACKAGE | POWDER | 20 | 9 | |
| 71052-064-25 | Toltrazuril | 0.025 kg in 1 PACKAGE | POWDER | 0.025 | 9 | |
| 71052-064-26 | Toltrazuril | 25 kg in 1 PACKAGE | POWDER | 25 | 9 | |
| 71052-064-50 | Toltrazuril | 0.5 kg in 1 PACKAGE | POWDER | 0.5 | 9 |
Products#
Every source-derived product name is available through these pages.
- Toltrazuril
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71052-064 | 71052-064-20, 71052-064-05, 71052-064-25, 71052-064-26, 71052-064-50, 71052-064-21 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Toltrazuril | QVZ3IAR3JS | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 8 | 2026-02-13 | monthly-update | 2026-06-03 17:56:51 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
