NDC 46066-504-48 - Tylosin Tartrate

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
46066-504
Requested NDC
46066-504-48
Package NDCs from labels
46066-504-47, 46066-504-48
Manufacturer
Aspen Veterinary Resources, LTD
Effective date
2025-03-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tylosin Tartrate - Aspen Veterinary Resources, LTDAspen Veterinary Resources, LTD2025-03-19PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46066-504-47Tylosin Tartrate100 g in 1 PACKETPOWDER, FOR SOLUTION10017
46066-504-48Tylosin Tartrate100 g in 1 JARPOWDER, FOR SOLUTION10017

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46066-504TYLOSIN TARTRATE POWDER, FOR SOLUTION [ASPEN VETERINARY RESOURCES, LTD]172 package rows20250322_63db6013-8bda-4d29-bb2d-bafb9777ceb7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TYLOSIN TARTRATEACTIVE INGREDIENT5P4625C51TTYLOSIN TARTRATE POWDER, FOR SOLUTION [ASPEN VETERINARY RESOURCES, LTD]1
TYLOSINACTIVE MOIETYYEF4JXN031TYLOSIN TARTRATE POWDER, FOR SOLUTION [ASPEN VETERINARY RESOURCES, LTD]1

Reported adverse events (FAERS/openFDA)#

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