Maropitant

Manufacturer
PROCOS SpA
Effective date
2022-03-22
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
4
Source
full-release
Hydrated at
2026-06-01 02:50:25

Label at a glance#

ProductMaropitant
Active ingredientMAROPITANT
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAROPITANT

CAS 147116-67-4

NDC 46016-1470-0

PROCOS SpA

Via Matteotti 249 Cameri - Italy

CAUTION

KEEP CONTAINERS TIGHTLY CLOSED

DO NOT EXPOSE THE SUBSTANCE TO LIGHT

CAUTION

FOR MANUFACTURING, PROCESSING OR REPACKING

FEDERAL LAW RESTRICTS THIS DRUG TO USE BY OR ON THE ORDER OF A LICENSED VETERINARIAN

Storage Conditions:

STORE AT 25°C, EXCURSIONS PERMITTED BETWEEN 15°C AND 30°C.

TRANSIENT SPIKES UP TO 40°C ARE ALSO PERMITTED.

label 1label 1

label 2label 2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46016-1470-0Maropitant50 kg in 1 CONTAINERPOWDER504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
46016-1470MAROPITANT POWDER [PROCOS SPA]41 package rows20220323_14091980-47cc-41cb-a75b-0671efd0d22d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46016-147046016-1470-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAROPITANT4XE2T9H4DHACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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