| NDC Code | 55150-175-01 |
|---|
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (55150-175-01) > 1 mL in 1 VIAL, SINGLE-USE |
|---|
| Product NDC | 55150-175 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Granisetron Hydrochloride |
|---|
| Non-Proprietary Name | Granisetron Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20160706 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204238 |
|---|
| Manufacturer | AuroMedics Pharma LLC |
|---|
| Substance Name | GRANISETRON HYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|