NDC 71052-064-26 - Toltrazuril
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
- 71052-064
- Requested NDC
- 71052-064-26
- Package NDCs from labels
- 71052-064-20, 71052-064-05, 71052-064-25, 71052-064-26, 71052-064-50, 71052-064-21
- Manufacturer
- DARMERICA, LLC
- Effective date
- 2026-04-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Toltrazuril - DARMERICA, LLC | DARMERICA, LLC | 2026-04-02 | BULK INGREDIENT - ANIMAL DRUG |
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 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.