Home > National Drug Code (NDC) > ONDANSETRON

ONDANSETRON - 62756-356-64 - (ONDANSETRON)

Alphabetical Index


Drug Information of ONDANSETRON

Product NDC: 62756-356
Proprietary Name: ONDANSETRON
Non Proprietary Name: ONDANSETRON
Active Ingredient(s): 8    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: 62756-356
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077557
Marketing Category: ANDA
Start Marketing Date: 20070802

Package Information of ONDANSETRON

Package NDC: 62756-356-64
Package Description: 3 BLISTER PACK in 1 DOSE PACK (62756-356-64) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of ONDANSETRON

NDC Code 62756-356-64
Proprietary Name ONDANSETRON
Package Description 3 BLISTER PACK in 1 DOSE PACK (62756-356-64) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 62756-356
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 Sun Pharmaceutical Industries Limited
Substance Name ONDANSETRON
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of ONDANSETRON


General Information