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ONDANSETRON
ONDANSETRON - 55289-559-06 - (ONDANSETRON)
Drug Information of ONDANSETRON
| Product NDC: | 55289-559 |
| Proprietary Name: | ONDANSETRON |
| Non Proprietary Name: | ONDANSETRON |
| Active Ingredient(s): | 4 mg/1 & nbsp; ONDANSETRON |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ONDANSETRON
| Product NDC: | 55289-559 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077557 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070802 |
Package Information of ONDANSETRON
| Package NDC: | 55289-559-06 |
| Package Description: | 6 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-559-06) > 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (55289-559-05) |
NDC Information of ONDANSETRON
| NDC Code | 55289-559-06 |
| Proprietary Name | ONDANSETRON |
| Package Description | 6 BOTTLE, PLASTIC in 1 BOTTLE, PLASTIC (55289-559-06) > 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (55289-559-05) |
| Product NDC | 55289-559 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ONDANSETRON |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20070802 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | ONDANSETRON |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
