Product NDC: | 43288-104 |
Proprietary Name: | Zuplenz |
Non Proprietary Name: | ONDANSETRON |
Active Ingredient(s): | 4 mg/1 & nbsp; ONDANSETRON |
Administration Route(s): | ORAL |
Dosage Form(s): | FILM, SOLUBLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43288-104 |
Labeler Name: | Praelia Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022524 |
Marketing Category: | NDA |
Start Marketing Date: | 20100705 |
Package NDC: | 43288-104-10 |
Package Description: | 10 POUCH in 1 BOX (43288-104-10) > 1 FILM, SOLUBLE in 1 POUCH (43288-104-01) |
NDC Code | 43288-104-10 |
Proprietary Name | Zuplenz |
Package Description | 10 POUCH in 1 BOX (43288-104-10) > 1 FILM, SOLUBLE in 1 POUCH (43288-104-01) |
Product NDC | 43288-104 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ONDANSETRON |
Dosage Form Name | FILM, SOLUBLE |
Route Name | ORAL |
Start Marketing Date | 20100705 |
Marketing Category Name | NDA |
Labeler Name | Praelia Pharmaceuticals Inc |
Substance Name | ONDANSETRON |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |