| NDC Code | 0054-0143-07 |
|---|
| Package Description | 20 TABLET in 1 BOTTLE (0054-0143-07) |
|---|
| Product NDC | 0054-0143 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Granisetron Hydrochloride |
|---|
| Non-Proprietary Name | Granisetron Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20071231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077842 |
|---|
| Manufacturer | West-Ward Pharmaceuticals Corp. |
|---|
| Substance Name | GRANISETRON HYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|