FDA.reportPublic FDA data

NDC 71052-190-20 - 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
71052-190
Requested NDC
71052-190-20
Package NDCs from labels
71052-190-20, 71052-190-05, 71052-190-00, 71052-190-10
Manufacturer
DARMERICA, LLC
Effective date
2026-01-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tylosin Tartrate - DARMERICA, LLCDARMERICA, LLC2026-01-09BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-190-00Tylosin Tartrate0.5 kg in 1 PACKAGEPOWDER0.54
71052-190-05Tylosin Tartrate5 kg in 1 PACKAGEPOWDER54
71052-190-10Tylosin Tartrate0.10 kg in 1 PACKAGEPOWDER0.104
71052-190-20Tylosin Tartrate1 kg in 1 PACKAGEPOWDER14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-190TYLOSIN TARTRATE POWDER [DARMERICA, LLC]34 package rows20241228_5b9135d8-e1f2-4a95-b05a-da7e52be8157.zip

Reported adverse events (FAERS/openFDA)#

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