NDC 10695-319 - 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
- 10695-319
- Package NDCs from labels
- 10695-319-50
- Manufacturer
- Willow Birch Pharma, LLC | Willow Birch Pharma, LLC. | Jiangsu Willing Bio-Tech Co., Ltd
- Effective date
- 2026-08-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ponazuril | Willow Birch Pharma, LLC | Willow Birch Pharma, LLC. | Jiangsu Willing Bio-Tech Co., Ltd | 2026-08-28 | BULK INGREDIENT - ANIMAL DRUG |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.