Product NDC: | 55154-2876 |
Proprietary Name: | Ondansetron |
Non Proprietary Name: | Ondansetron |
Active Ingredient(s): | 2 mg/mL & nbsp; Ondansetron |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-2876 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077541 |
Marketing Category: | ANDA |
Start Marketing Date: | 20061226 |
Package NDC: | 55154-2876-5 |
Package Description: | 5 VIAL in 1 BAG (55154-2876-5) > 2 mL in 1 VIAL |
NDC Code | 55154-2876-5 |
Proprietary Name | Ondansetron |
Package Description | 5 VIAL in 1 BAG (55154-2876-5) > 2 mL in 1 VIAL |
Product NDC | 55154-2876 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ondansetron |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20061226 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |