FDA.reportPublic FDA data

NDC 62991-3152-2 - 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
62991-3152
Requested NDC
62991-3152-2
Package NDCs from labels
62991-3152-1, 62991-3152-2, 62991-3152-3, 62991-3152-4, 62991-3152-5
Manufacturer
LETCO MEDICAL, LLC
Effective date
2026-06-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
TYLOSIN TARTRATE - LETCO MEDICAL, LLCLETCO MEDICAL, LLC2026-06-05BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62991-3152-1TYLOSIN TARTRATE25 g in 1 JARPOWDER257
62991-3152-2TYLOSIN TARTRATE100 g in 1 JARPOWDER1007
62991-3152-3TYLOSIN TARTRATE500 g in 1 JARPOWDER5007
62991-3152-4TYLOSIN TARTRATE1000 g in 1 JARPOWDER10007
62991-3152-5TYLOSIN TARTRATE15000 g in 1 DRUMPOWDER150007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62991-3152TYLOSIN TARTRATE POWDER [LETCO MEDICAL, LLC]65 package rows20240719_c8a73a48-f436-464a-b831-ef62cf6dfea1.zip

Reported adverse events (FAERS/openFDA)#

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