NDC 86236-001-01 - DICLAZURIL
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
- 86236-001
- Requested NDC
- 86236-001-01
- Package NDCs from labels
- 86236-001-01, 86236-001-02, 86236-001-03, 86236-001-04, 86236-001-05
- Manufacturer
- Chongqing VPON Pharmaceutical Co., Ltd.
- Effective date
- 2026-06-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 86236-(001-002) | Chongqing VPON Pharmaceutical Co., Ltd. | 2026-06-24 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86236-001-01 | DICLAZURIL | 1 kg in 1 BAG | POWDER | 1 | 2 | |
| 86236-001-02 | DICLAZURIL | 5 kg in 1 BAG | POWDER | 5 | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.