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Ondansetron
Ondansetron - 54838-555-50 - (Ondansetron Hydrochloride)
Drug Information of Ondansetron
| Product NDC: | 54838-555 |
| Proprietary Name: | Ondansetron |
| Non Proprietary Name: | Ondansetron Hydrochloride |
| Active Ingredient(s): | 4 mg/5mL & nbsp; Ondansetron Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ondansetron
| Product NDC: | 54838-555 |
| Labeler Name: | Silarx Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091342 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110127 |
Package Information of Ondansetron
| Package NDC: | 54838-555-50 |
| Package Description: | 50 mL in 1 BOTTLE, PLASTIC (54838-555-50) |
NDC Information of Ondansetron
| NDC Code | 54838-555-50 |
| Proprietary Name | Ondansetron |
| Package Description | 50 mL in 1 BOTTLE, PLASTIC (54838-555-50) |
| Product NDC | 54838-555 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ondansetron Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20110127 |
| Marketing Category Name | ANDA |
| Labeler Name | Silarx Pharmaceuticals, Inc |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
