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ONDANSETRON HYDROCHLORIDE
ONDANSETRON HYDROCHLORIDE - 62756-181-01 - (ONDANSETRON HYDROCHLORIDE)
Drug Information of ONDANSETRON HYDROCHLORIDE
| Product NDC: | 62756-181 |
| 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: | 62756-181 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077173 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061226 |
Package Information of ONDANSETRON HYDROCHLORIDE
| Package NDC: | 62756-181-01 |
| Package Description: | 5 AMPULE in 1 CARTON (62756-181-01) > 2 mL in 1 AMPULE |
NDC Information of ONDANSETRON HYDROCHLORIDE
| NDC Code | 62756-181-01 |
| Proprietary Name | ONDANSETRON HYDROCHLORIDE |
| Package Description | 5 AMPULE in 1 CARTON (62756-181-01) > 2 mL in 1 AMPULE |
| Product NDC | 62756-181 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ONDANSETRON HYDROCHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20061226 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
