NDC 0859-2159 - Drontal Plus
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
- 0859-2159
- Package NDCs from labels
- 0859-2159-01
- Manufacturer
- Bayer HealthCare LLC Animal Health Division
- Effective date
- 2021-11-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drontal Plus - Bayer HealthCare LLC Animal Health Division | Bayer HealthCare LLC Animal Health Division | 2021-11-04 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FEBANTEL | ACTIVE INGREDIENT | S75C401OS1 | DRONTAL PLUS (PRAZIQUANTEL/PYRANTEL PAMOATE/FEBANTEL) TABLET [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 3 | |
| PRAZIQUANTEL | ACTIVE INGREDIENT | 6490C9U457 | DRONTAL PLUS (PRAZIQUANTEL/PYRANTEL PAMOATE/FEBANTEL) TABLET [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 3 | |
| PYRANTEL PAMOATE | ACTIVE INGREDIENT | 81BK194Z5M | DRONTAL PLUS (PRAZIQUANTEL/PYRANTEL PAMOATE/FEBANTEL) TABLET [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 3 | |
| FEBANTEL | ACTIVE MOIETY | S75C401OS1 | DRONTAL PLUS (PRAZIQUANTEL/PYRANTEL PAMOATE/FEBANTEL) TABLET [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 3 | |
| PRAZIQUANTEL | ACTIVE MOIETY | 6490C9U457 | DRONTAL PLUS (PRAZIQUANTEL/PYRANTEL PAMOATE/FEBANTEL) TABLET [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 3 | |
| PYRANTEL | ACTIVE MOIETY | 4QIH0N49E7 | DRONTAL PLUS (PRAZIQUANTEL/PYRANTEL PAMOATE/FEBANTEL) TABLET [BAYER HEALTHCARE LLC ANIMAL HEALTH DIVISION] | 3 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.