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ONDANSETRON HYDROCHLORIDE
ONDANSETRON HYDROCHLORIDE - 21695-834-15 - (ONDANSETRON HYDROCHLORIDE)
Drug Information of ONDANSETRON HYDROCHLORIDE
| Product NDC: | 21695-834 |
| Proprietary Name: | ONDANSETRON HYDROCHLORIDE |
| Non Proprietary Name: | ONDANSETRON HYDROCHLORIDE |
| Active Ingredient(s): | 4 mg/1 & nbsp; ONDANSETRON HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ONDANSETRON HYDROCHLORIDE
| Product NDC: | 21695-834 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077050 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070625 |
Package Information of ONDANSETRON HYDROCHLORIDE
| Package NDC: | 21695-834-15 |
| Package Description: | 15 TABLET, FILM COATED in 1 BOTTLE (21695-834-15) |
NDC Information of ONDANSETRON HYDROCHLORIDE
| NDC Code | 21695-834-15 |
| Proprietary Name | ONDANSETRON HYDROCHLORIDE |
| Package Description | 15 TABLET, FILM COATED in 1 BOTTLE (21695-834-15) |
| Product NDC | 21695-834 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ONDANSETRON HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070625 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ONDANSETRON HYDROCHLORIDE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
