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Ondansetron Hydrochloride
Ondansetron Hydrochloride - 0527-1726-41 - (Ondansetron Hydrochloride)
Drug Information of Ondansetron Hydrochloride
| Product NDC: | 0527-1726 |
| 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): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ondansetron Hydrochloride
| Product NDC: | 0527-1726 |
| Labeler Name: | Lannett Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090116 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100701 |
Package Information of Ondansetron Hydrochloride
| Package NDC: | 0527-1726-41 |
| Package Description: | 5 VIAL, SINGLE-DOSE in 1 CARTON (0527-1726-41) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Ondansetron Hydrochloride
| NDC Code | 0527-1726-41 |
| Proprietary Name | Ondansetron Hydrochloride |
| Package Description | 5 VIAL, SINGLE-DOSE in 1 CARTON (0527-1726-41) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0527-1726 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ondansetron Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20100701 |
| Marketing Category Name | ANDA |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
