NDC 13985-612 - XylaMed
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
- 13985-612
- Package NDCs from labels
- 13985-612-50
- Manufacturer
- MWI/Vet One | Bimeda Inc. | Bimeda MTC Animal Health
- Effective date
- 2018-12-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| XylaMed - MWI/Vet One | Bimeda Inc. | Bimeda MTC Animal Health | MWI/Vet One | Bimeda Inc. | Bimeda MTC Animal Health | 2018-12-11 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| XYLAZINE | ACTIVE INGREDIENT | 2KFG9TP5V8 | XYLAMED (XYLAZINE) INJECTION, SOLUTION [MWI/VET ONE] | 2 | |
| XYLAZINE | ACTIVE MOIETY | 2KFG9TP5V8 | XYLAMED (XYLAZINE) INJECTION, SOLUTION [MWI/VET ONE] | 2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.