NDC 86252-001-01 - Florfenicol
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
- 86252-001
- Requested NDC
- 86252-001-01
- Package NDCs from labels
- 86252-001-01
- Manufacturer
- Suzhou Muyuanda Biotechnology Co., Ltd
- Effective date
- 2026-02-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Florfenicol - Suzhou Muyuanda Biotechnology Co., Ltd | Suzhou Muyuanda Biotechnology Co., Ltd | 2026-02-22 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86252-001-01 | Florfenicol | 500 mg in 1 BAG | POWDER | 500 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.