FDA.reportPublic FDA data

NDC 23243-7287-1 - Tilmovet AC Oral Solution

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
23243-7287
Requested NDC
23243-7287-1
Package NDCs from labels
23243-7287-1
Manufacturer
Huvepharma, Inc.
Effective date
2025-09-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tilmovet AC Oral Solution - Huvepharma, Inc.Huvepharma, Inc.2025-09-24PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-7287-1Tilmovet ACOral Solution960 mL in 1 BOTTLECONCENTRATE9603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-7287TILMOVET AC ORAL SOLUTION (TILMICOSIN PHOSPHATE) CONCENTRATE [HUVEPHARMA, INC.]11 package rows20220129_50992c16-6637-4e13-9aa0-a3b9fedf9d27.zip

Reported adverse events (FAERS/openFDA)#

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