Home > National Drug Code (NDC) > Ondansetron

Ondansetron - 0904-6208-46 - (Ondansetron hydrochloride)

Alphabetical Index


Drug Information of Ondansetron

Product NDC: 0904-6208
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron hydrochloride
Active Ingredient(s): 4    mg/1 & nbsp;   Ondansetron hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 0904-6208
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077545
Marketing Category: ANDA
Start Marketing Date: 20080101

Package Information of Ondansetron

Package NDC: 0904-6208-46
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0904-6208-46)

NDC Information of Ondansetron

NDC Code 0904-6208-46
Proprietary Name Ondansetron
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0904-6208-46)
Product NDC 0904-6208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080101
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


General Information