NDC Code | 0069-1340-16 |
Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-1340-16) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-1340-05) |
Product NDC | 0069-1340 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ondansetron Hydrochloride |
Non-Proprietary Name | Ondansetron Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20110510 |
Marketing Category Name | ANDA |
Application Number | ANDA078244 |
Manufacturer | Pfizer Laboratories Div Pfizer Inc |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength | 2 |
Strength Unit | mg/mL |
Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |