FDA.reportPublic FDA data

NDC 71052-023-25 - Clenbuterol HCl

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
71052-023
Requested NDC
71052-023-25
Package NDCs from labels
71052-023-05, 71052-023-10, 71052-023-25
Manufacturer
DARMERICA, LLC
Effective date
2024-01-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Clenbuterol HCl - DARMERICA, LLCDARMERICA, LLC2024-01-08BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-023-05Clenbuterol HCl5 g in 1 PACKAGEPOWDER51
71052-023-10Clenbuterol HCl100 g in 1 PACKAGEPOWDER1001
71052-023-25Clenbuterol HCl25 g in 1 PACKAGEPOWDER251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-023CLENBUTEROL HCL POWDER [DARMERICA, LLC]13 package rows20240109_428f324f-a429-45ca-bfcb-abb7fcf5ce18.zip

Reported adverse events (FAERS/openFDA)#

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