NDC 0010-3831 - Synanthic Bovine Dewormer
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
- 0010-3831
- Package NDCs from labels
- 0010-3831-01, 0010-3831-02
- Manufacturer
- Boehringer Ingelheim Animal Health USA Inc.
- Effective date
- 2021-12-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Synanthic ® oxfendazole oral suspension Bovine Dewormer Suspension, 9.06% | Boehringer Ingelheim Animal Health USA Inc. | 2021-12-30 | OTC ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| OXFENDAZOLE | ACTIVE INGREDIENT | OMP2H17F9E | SYNANTHIC BOVINE DEWORMER (OXFENDAZOLE) SUSPENSION [BOEHRINGER INGELHEIM VETMEDICA, INC.] | 3 | |
| OXFENDAZOLE | ACTIVE MOIETY | OMP2H17F9E | SYNANTHIC BOVINE DEWORMER (OXFENDAZOLE) SUSPENSION [BOEHRINGER INGELHEIM VETMEDICA, INC.] | 3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.