NDC 71052-068 - Ponazuril
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
- 71052-068
- Package NDCs from labels
- 71052-068-01, 71052-068-15, 71052-068-10, 71052-068-02, 71052-068-05, 71052-068-25
- Manufacturer
- DARMERICA, LLC
- Effective date
- 2026-09-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ponazuril - DARMERICA, LLC | DARMERICA, LLC | 2026-09-09 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71052-068-01 | Ponazuril | 1 kg in 1 PACKAGE | POWDER | 1 | 7 | |
| 71052-068-02 | Ponazuril | 0.05 kg in 1 PACKAGE | POWDER | 0.05 | 7 | |
| 71052-068-05 | Ponazuril | 5 kg in 1 PACKAGE | POWDER | 5 | 7 | |
| 71052-068-10 | Ponazuril | 0.1 kg in 1 PACKAGE | POWDER | 0.1 | 7 | |
| 71052-068-15 | Ponazuril | 0.5 kg in 1 PACKAGE | POWDER | 0.5 | 7 | |
| 71052-068-25 | Ponazuril | 25 kg in 1 PACKAGE | POWDER | 25 | 7 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.