NDC 58198-0029-1 - Cydectin

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
58198-0029
Requested NDC
58198-0029-1
Package NDCs from labels
58198-0029-1, 58198-0029-2
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
LabelManufacturerEffective dateType
Cydectin - Elanco US Inc.Elanco US Inc.2026-07-22OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58198-0029-1Cydectin1000 mL in 1 BOTTLELIQUID10005
58198-0029-2Cydectin4000 mL in 1 BOTTLELIQUID40005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58198-0029CYDECTIN (MOXIDECTIN) LIQUID [ELANCO US INC.]52 package rows20250206_aa2d9a4d-a442-4d1c-a7bd-17b09d8ab718.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MoxidectinMOXIDECTINMedicines Development for Global Health6eb02ae9-9065-176f-e053-2991aa0ac8912026-07-30Warnings, Adverse reactionsExact identifier
unii: NGU5H31YO9

Reported adverse events (FAERS/openFDA)#

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