FDA.reportPublic FDA data

NDC 71052-372 - Aminopentamide Sulfate

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
71052-372
Package NDCs from labels
71052-372-25, 71052-372-10
Manufacturer
DARMERICA, LLC
Effective date
2026-10-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Aminopentamide Sulfate - DARMERICA, LLCDARMERICA, LLC2026-10-07BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-372-10Aminopentamide Sulfate0.010 kg in 1 PACKAGEPOWDER0.0103
71052-372-25Aminopentamide Sulfate0.025 kg in 1 PACKAGEPOWDER0.0253

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-372AMINOPENTAMIDE SULFATE POWDER [DARMERICA, LLC]32 package rows20241222_22e62d5a-e5f9-4def-9f8b-a3a8f67eeb86.zip

Reported adverse events (FAERS/openFDA)#

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