NDC Code | 0078-0680-19 |
Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0680-19) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0078-0680-61) |
Product NDC | 0078-0680 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Zofran |
Proprietary Name Suffix | Odt |
Non-Proprietary Name | Ondansetron Hydrochloride |
Dosage Form | TABLET, ORALLY DISINTEGRATING |
Usage | ORAL |
Start Marketing Date | 20170823 |
End Marketing Date | 20191031 |
Marketing Category Name | NDA |
Application Number | NDA020781 |
Manufacturer | Novartis Pharmaceuticals Corporation |
Substance Name | ONDANSETRON |
Strength | 8 |
Strength Unit | mg/1 |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |