NDC Code | 61786-693-15 |
Package Description | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-693-15) |
Product NDC | 61786-693 |
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 | 20160519 |
Marketing Category Name | ANDA |
Application Number | ANDA078539 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength | 4 |
Strength Unit | mg/1 |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |