| NDC Code | 52584-069-00 |
|---|
| Package Description | 1 VIAL, SINGLE-USE in 1 BAG (52584-069-00) > 2 mL in 1 VIAL, SINGLE-USE |
|---|
| Product NDC | 52584-069 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ondansetron |
|---|
| Non-Proprietary Name | Ondansetron |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20180703 |
|---|
| End Marketing Date | 20231130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203711 |
|---|
| Manufacturer | General Injectables and Vaccines, Inc. |
|---|
| Substance Name | ONDANSETRON HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC] |
|---|