Home
>
National Drug Code (NDC)
>
ONDANSETRON HYDROCHLORIDE
ONDANSETRON HYDROCHLORIDE - 36000-012-25 - (ONDANSETRON HYDROCHLORIDE)
Drug Information of ONDANSETRON HYDROCHLORIDE
| Product NDC: | 36000-012 |
| 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: | 36000-012 |
| Labeler Name: | Claris Lifesciences Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078287 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130313 |
Package Information of ONDANSETRON HYDROCHLORIDE
| Package NDC: | 36000-012-25 |
| Package Description: | 25 VIAL in 1 CARTON (36000-012-25) > 2 mL in 1 VIAL |
NDC Information of ONDANSETRON HYDROCHLORIDE
| NDC Code | 36000-012-25 |
| Proprietary Name | ONDANSETRON HYDROCHLORIDE |
| Package Description | 25 VIAL in 1 CARTON (36000-012-25) > 2 mL in 1 VIAL |
| Product NDC | 36000-012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ONDANSETRON HYDROCHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20130313 |
| Marketing Category Name | ANDA |
| Labeler Name | Claris Lifesciences Inc. |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
