NDC Code | 35356-445-30 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-445-30) |
Product NDC | 35356-445 |
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 | 20111103 |
Marketing Category Name | ANDA |
Application Number | ANDA076252 |
Manufacturer | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength | 8 |
Strength Unit | mg/1 |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |