NDC 86228-001-01 - 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
- 86228-001
- Requested NDC
- 86228-001-01
- Package NDCs from labels
- 86228-001-01
- Manufacturer
- Shanghai Zhenhong Pharm Tech Co., Ltd.
- Effective date
- 2025-04-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 86228-001 | Shanghai Zhenhong Pharm Tech Co., Ltd. | 2025-04-28 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.