Home > National Drug Code (NDC) > ONDANSETRON

ONDANSETRON - 55289-559-06 - (ONDANSETRON)

Alphabetical Index


Drug Information of ONDANSETRON

Product NDC: 55289-559
Proprietary Name: ONDANSETRON
Non Proprietary Name: ONDANSETRON
Active Ingredient(s): 4    mg/1 & nbsp;   ONDANSETRON
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of ONDANSETRON

Product NDC: 55289-559
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077557
Marketing Category: ANDA
Start Marketing Date: 20070802

Package Information of ONDANSETRON

Package NDC: 55289-559-06
Package Description: 6 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-559-06) > 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (55289-559-05)

NDC Information of ONDANSETRON

NDC Code 55289-559-06
Proprietary Name ONDANSETRON
Package Description 6 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-559-06) > 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (55289-559-05)
Product NDC 55289-559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ONDANSETRON
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20070802
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name ONDANSETRON
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