Home NDC 58198-0470 NDC 58198-0470 - Pulmotil AC 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 58198-0470
Package NDCs from labels 58198-0470-1
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 Pulmotil AC - 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 58198-0470-1 Pulmotil AC 960 mL in 1 BOTTLE CONCENTRATE 960 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58198-0470 PULMOTIL AC (TILMICOSIN PHOSPHATE) CONCENTRATE [ELANCO US INC.] 9 1 package rows 20250114_f4267d77-6a81-491e-9ae5-8cbccc99339c.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.