NDC 0859-2351-02 - Veraflox
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
- 0859-2351
- Requested NDC
- 0859-2351-02
- Package NDCs from labels
- 0859-2351-01, 0859-2351-03, 0859-2351-02, 0859-2351-04
- Manufacturer
- Bayer HealthCare LLC Animal Health Division
- Effective date
- 2020-12-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Veraflox - Bayer HealthCare LLC Animal Health Division | Bayer HealthCare LLC Animal Health Division | 2020-12-02 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PRADOFLOXACIN | ACTIVE INGREDIENT | 6O0T5E048I | VERAFLOX (PRADOFLOXACIN) SUSPENSION [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 1 | |
| PRADOFLOXACIN | ACTIVE MOIETY | 6O0T5E048I | VERAFLOX (PRADOFLOXACIN) SUSPENSION [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.