Home NDC 58198-1300-1 NDC 58198-1300-1 - Tylan Soluble 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 58198-1300
Requested NDC 58198-1300-1
Package NDCs from labels 58198-1300-1
Manufacturer Elanco US Inc.
Effective date 2025-11-21
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Tylan Soluble - Elanco US Inc. Elanco US Inc. 2025-11-21 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-1300-1 Tylan Soluble 3785 mL in 1 BOTTLE, PLASTIC POWDER 3785 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-1300 TYLAN SOLUBLE (TYLOSIN TARTRATE) POWDER [ELANCO US INC.] 6 1 package rows 20250114_0c3d01b7-be57-4031-adbe-5dbdd2a6d7f2.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.