NDC Code | 68084-221-01 |
Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-221-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11) |
Product NDC | 68084-221 |
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 | 20230801 |
Marketing Category Name | ANDA |
Application Number | ANDA078539 |
Manufacturer | American Health Packaging |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength | 8 |
Strength Unit | mg/1 |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |