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Ondansetron Hydrochloride
Ondansetron Hydrochloride - 23155-168-31 - (Ondansetron Hydrochloride)
Drug Information of Ondansetron Hydrochloride
| Product NDC: | 23155-168 |
| Proprietary Name: | Ondansetron Hydrochloride |
| Non Proprietary Name: | Ondansetron Hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; Ondansetron Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ondansetron Hydrochloride
| Product NDC: | 23155-168 |
| Labeler Name: | Heritage Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090424 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121213 |
Package Information of Ondansetron Hydrochloride
| Package NDC: | 23155-168-31 |
| Package Description: | 1 VIAL in 1 PACKAGE (23155-168-31) > 20 mL in 1 VIAL |
NDC Information of Ondansetron Hydrochloride
| NDC Code | 23155-168-31 |
| Proprietary Name | Ondansetron Hydrochloride |
| Package Description | 1 VIAL in 1 PACKAGE (23155-168-31) > 20 mL in 1 VIAL |
| Product NDC | 23155-168 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ondansetron Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20121213 |
| Marketing Category Name | ANDA |
| Labeler Name | Heritage Pharmaceuticals Inc. |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
