FDA.reportPublic FDA data

NDC 71052-037-50 - Domperidone

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
71052-037
Requested NDC
71052-037-50
Package NDCs from labels
71052-037-05, 71052-037-50, 71052-037-10, 71052-037-01
Manufacturer
DARMERICA, LLC
Effective date
2026-01-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Domperidone - DARMERICA, LLCDARMERICA, LLC2026-01-07BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-037-01Domperidone1 kg in 1 PACKAGEPOWDER16
71052-037-05Domperidone05 kg in 1 PACKAGEPOWDER056
71052-037-10Domperidone0.1 kg in 1 PACKAGEPOWDER0.16
71052-037-50Domperidone0.5 kg in 1 PACKAGEPOWDER0.56

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-037DOMPERIDONE POWDER [DARMERICA, LLC]54 package rows20250413_cdb0c9b9-388c-4a06-9fe9-bb4e52278a4e.zip

Reported adverse events (FAERS/openFDA)#

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