Product NDC: | 43063-247 |
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) |
Product NDC: | 43063-247 |
Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077557 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070802 |
Package NDC: | 43063-247-01 |
Package Description: | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-247-01) |
NDC Code | 43063-247-01 |
Proprietary Name | ONDANSETRON |
Package Description | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-247-01) |
Product NDC | 43063-247 |
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] |