| NDC Code | 51655-933-87 |
|---|
| Package Description | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87) |
|---|
| Product NDC | 51655-933 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron Hydrochloride |
|---|
| Non-Proprietary Name | Ondansetron Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220720 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078539 |
|---|
| Manufacturer | Northwind Pharmaceuticals, LLC |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|