NDC 54771-1006 - Mitaban
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
- 54771-1006
- Package NDCs from labels
- 54771-1006-1
- Manufacturer
- Zoetis Inc.
- Effective date
- 2018-03-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Mitaban ® amitraz | Zoetis Inc. | 2018-03-01 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| amitraz | ACTIVE INGREDIENT | 33IAH5017S | MITABAN (AMITRAZ) LIQUID [ZOETIS INC.] | 1 | |
| amitraz | ACTIVE MOIETY | 33IAH5017S | MITABAN (AMITRAZ) LIQUID [ZOETIS INC.] | 1 | |
| o-xylene | INACTIVE INGREDIENT | Z2474E14QP | MITABAN (AMITRAZ) LIQUID [ZOETIS INC.] | 1 | |
| propylene oxide | INACTIVE INGREDIENT | Y4Y7NYD4BK | MITABAN (AMITRAZ) LIQUID [ZOETIS INC.] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.