Home NDC 58198-0230-2 NDC 58198-0230-2 - Micotil 300 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 58198-0230
Requested NDC 58198-0230-2
Package NDCs from labels 58198-0230-2
Manufacturer Elanco US Inc.
Effective date 2026-07-22
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Micotil 300 - Elanco US Inc. Elanco US Inc. 2026-07-22 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58198-0230-2 Micotil 300 250 mL in 1 BOTTLE, GLASS INJECTION 250 7 58198-0230-2 Micotil 300 1 in 1 CARTON INJECTION 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0230 MICOTIL 300 (TILMICOSIN PHOSPHATE) INJECTION [ELANCO US INC.] 6 2 package rows 20250207_08f1aecd-33c2-457b-8a45-c38fafb3a1c7.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.