NDC 71052-114 - Maropitant Citrate

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
71052-114
Package NDCs from labels
71052-114-01, 71052-114-25, 71052-114-50, 71052-114-10, 71052-114-11
Manufacturer
DARMERICA, LLC
Effective date
2024-07-25
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Maropitant Citrate - DARMERICA, LLCDARMERICA, LLC2024-07-25BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-114-01Maropitant Citrate0.010 kg in 1 PACKAGEPOWDER0.0102
71052-114-10Maropitant Citrate0.10 kg in 1 PACKAGEPOWDER0.102
71052-114-11Maropitant Citrate1 kg in 1 PACKAGEPOWDER12
71052-114-25Maropitant Citrate0.025 kg in 1 PACKAGEPOWDER0.0252
71052-114-50Maropitant Citrate0.050 kg in 1 PACKAGEPOWDER0.0502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-114MAROPITANT CITRATE POWDER [DARMERICA, LLC]25 package rows20240726_a2b8c500-f1b3-4abd-ab9d-1dd8e01adad9.zip