Product NDC: | 54868-5888 |
Proprietary Name: | Ondansetron |
Non Proprietary Name: | Ondansetron Hydrochloride |
Active Ingredient(s): | 2 mg/mL & nbsp; Ondansetron Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5888 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076781 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080508 |
Package NDC: | 54868-5888-0 |
Package Description: | 5 VIAL in 1 CARTON (54868-5888-0) > 2 mL in 1 VIAL |
NDC Code | 54868-5888-0 |
Proprietary Name | Ondansetron |
Package Description | 5 VIAL in 1 CARTON (54868-5888-0) > 2 mL in 1 VIAL |
Product NDC | 54868-5888 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ondansetron Hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20080508 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ONDANSETRON HYDROCHLORIDE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |