Home
>
National Drug Code (NDC)
>
Ondansetron
Ondansetron - 0904-6208-46 - (Ondansetron hydrochloride)
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] |
