ONDANSETRON HCL DIHYDRATE powder

Ondansetron HCl Dihydrate by

Drug Labeling and Warnings

Ondansetron HCl Dihydrate by is a Other medication manufactured, distributed, or labeled by AX Pharmaceutical Corp, NATCO PHARMA LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Ondansetron HCl Dihydrate

INGREDIENTS AND APPEARANCE

ONDANSETRON HCL DIHYDRATE 
ondansetron hcl dihydrate powder

Product Information
Product Type		Item Code (Source)	NDC: 73377-325
Route of Administration	NOT APPLICABLE

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ONDANSETRON HYDROCHLORIDE (UNII: NMH84OZK2B) (ONDANSETRON - UNII:4AF302ESOS)	ONDANSETRON	1 g  in 1 g

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73377-325-01	100 g in 1 JAR
2	NDC: 73377-325-02	500 g in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
bulk ingredient for animal drug compounding		06/20/2025

Labeler - AX Pharmaceutical Corp (204011316)

Establishment
Name	Address	ID/FEI	Business Operations
AX Pharmaceutical Corp		204011316	label, pack, relabel, repack

Establishment
Name	Address	ID/FEI	Business Operations
NATCO PHARMA LIMITED		862497174	api manufacture