NDC Code | 0179-0248-44 |
Package Description | 1440 TABLET, FILM COATED in 1 BOTTLE (0179-0248-44) |
Product NDC | 0179-0248 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ondansetron Hydrochloride |
Non-Proprietary Name | Ondansetron Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20180830 |
End Marketing Date | 20200731 |
Marketing Category Name | ANDA |
Application Number | ANDA078539 |
Manufacturer | KAISER FOUNDATION HOSPITALS |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength | 8 |
Strength Unit | mg/1 |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |