NDC 73377-111-06 - Maropitant Citrate Hydrate

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: 73377-111
Requested NDC: 73377-111-06
Package NDCs from labels: 73377-111-01, 73377-111-02, 73377-111-03, 73377-111-04, 73377-111-05, 73377-111-06, 73377-111-07
Manufacturer: AX Pharmaceutical Corp
Effective date: 2026-03-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Maropitant Citrate Hydrate - AX Pharmaceutical Corp	AX Pharmaceutical Corp	2026-03-10	BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73377-111-01	Maropitant Citrate Hydrate	500 g in 1 JAR	POWDER	500	5
73377-111-02	Maropitant Citrate Hydrate	100 g in 1 JAR	POWDER	100	5
73377-111-03	Maropitant Citrate Hydrate	10 g in 1 JAR	POWDER	10	5
73377-111-04	Maropitant Citrate Hydrate	1000 g in 1 JAR	POWDER	1000	5
73377-111-05	Maropitant Citrate Hydrate	25 g in 1 JAR	POWDER	25	5
73377-111-06	Maropitant Citrate Hydrate	250 g in 1 JAR	POWDER	250	5
73377-111-07	Maropitant Citrate Hydrate	8 g in 1 JAR	POWDER	8	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73377-111	MAROPITANT CITRATE HYDRATE POWDER [AX PHARMACEUTICAL CORP]	3	7 package rows	20240823_e1ec11e2-330e-4098-8df7-aef3d7682913.zip

Reported adverse events (FAERS/openFDA)#

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