NDC Code | 51672-4108-6 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (51672-4108-6) |
Product NDC | 51672-4108 |
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 | 20110328 |
Marketing Category Name | ANDA |
Application Number | ANDA077729 |
Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength | 4 |
Strength Unit | mg/1 |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |