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