FDA.reportPublic FDA data

NDC 71052-119-01 - Decoquinate

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
71052-119
Requested NDC
71052-119-01
Package NDCs from labels
71052-119-01
Manufacturer
DARMERICA, LLC
Effective date
2025-04-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Decoquinate - DARMERICA, LLCDARMERICA, LLC2025-04-11BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-119-01Decoquinate1 kg in 1 PACKAGEPOWDER15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-119DECOQUINATE POWDER [DARMERICA, LLC]51 package rows20250413_65a5b191-146b-4e2d-8946-fbe9cdcff0c6.zip

Reported adverse events (FAERS/openFDA)#

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