FDA.reportPublic FDA data

NDC 51072-092 - TiaGard 12.5%

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
51072-092
Package NDCs from labels
51072-092-00, 51072-092-01, 51072-092-02
Manufacturer
Aurora Pharmaceutical, Inc.
Effective date
2024-06-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
TiaGard ® 12.5% (tiamulin hydrogen fumarate)Aurora Pharmaceutical, Inc.2024-06-19OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51072-092-00TiaGard 12.5%1000 mL in 1 BOTTLECONCENTRATE10009
51072-092-01TiaGard 12.5%5000 mL in 1 BOTTLECONCENTRATE50009
51072-092-02TiaGard 12.5%1000 mL in 1 BOTTLECONCENTRATE10009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51072-092TIAGARD 12.5% (TIAMULIN FUMARATE) CONCENTRATE [AURORA PHARMACEUTICAL, INC.]93 package rows20240702_556bba0f-4636-4fe9-beb2-7f53878d85b3.zip

Reported adverse events (FAERS/openFDA)#

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