Home NDC 58198-0206-3 NDC 58198-0206-3 - Tylan 200 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 58198-0206
Requested NDC 58198-0206-3
Package NDCs from labels 58198-0206-3, 58198-0206-5
Manufacturer Elanco US Inc.
Effective date 2025-07-25
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Tylan 200 - Elanco US Inc. Elanco US Inc. 2025-07-25 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-0206-3 Tylan 200 250 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 250 7 58198-0206-3 Tylan 200 1 in 1 CARTON INJECTION, SOLUTION 1 7 58198-0206-5 Tylan 200 500 mL in 1 BOTTLE, GLASS INJECTION, SOLUTION 500 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0206 TYLAN 200 (TYLOSIN) INJECTION, SOLUTION [ELANCO US INC.] 6 3 package rows 20231115_510b4ec0-6762-4b29-9786-e5afa7350fa3.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.