Product NDC: | 63629-4093 |
Proprietary Name: | ONDANSETRON HYDROCHLORIDE |
Non Proprietary Name: | ONDANSETRON HYDROCHLORIDE |
Active Ingredient(s): | 8 mg/1 & nbsp; ONDANSETRON HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-4093 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077050 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070625 |
Package NDC: | 63629-4093-0 |
Package Description: | 5 TABLET, FILM COATED in 1 BOTTLE (63629-4093-0) |
NDC Code | 63629-4093-0 |
Proprietary Name | ONDANSETRON HYDROCHLORIDE |
Package Description | 5 TABLET, FILM COATED in 1 BOTTLE (63629-4093-0) |
Product NDC | 63629-4093 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ONDANSETRON HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20070625 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength Number | 8 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |