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ondansetron hydrochloride
ondansetron hydrochloride - 25021-782-20 - (ondansetron hydrochloride)
Drug Information of ondansetron hydrochloride
| Product NDC: | 25021-782 |
| Proprietary Name: | ondansetron hydrochloride |
| Non Proprietary Name: | ondansetron hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; ondansetron hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ondansetron hydrochloride
| Product NDC: | 25021-782 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090648 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120830 |
Package Information of ondansetron hydrochloride
| Package NDC: | 25021-782-20 |
| Package Description: | 1 VIAL in 1 CARTON (25021-782-20) > 20 mL in 1 VIAL |
NDC Information of ondansetron hydrochloride
| NDC Code | 25021-782-20 |
| Proprietary Name | ondansetron hydrochloride |
| Package Description | 1 VIAL in 1 CARTON (25021-782-20) > 20 mL in 1 VIAL |
| Product NDC | 25021-782 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ondansetron hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20120830 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
