NDC 57561-232 - PROHIBIT

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
57561-232
Package NDCs from labels
57561-232-05, 57561-232-60
Manufacturer
Agri Laboratories, Ltd.
Effective date
2018-10-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PROHIBITAgri Laboratories, Ltd.2018-10-19OTC ANIMAL DRUG LABEL

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.