NDC 0859-2141-02 - Baytril
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
- 0859-2141
- Requested NDC
- 0859-2141-02
- Package NDCs from labels
- 0859-2141-01, 0859-2141-02
- Manufacturer
- Bayer HealthCare LLC Animal Health Division
- Effective date
- 2021-11-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Baytril - Bayer HealthCare LLC Animal Health Division | Bayer HealthCare LLC Animal Health Division | 2021-11-05 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ENROFLOXACIN | ACTIVE INGREDIENT | 3DX3XEK1BN | BAYTRIL (ENROFLOXACIN) TABLET, FILM COATED [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 4 | |
| ENROFLOXACIN | ACTIVE MOIETY | 3DX3XEK1BN | BAYTRIL (ENROFLOXACIN) TABLET, FILM COATED [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.