| NDC Code: |
25021-782 |
| Proprietary Name: |
ondansetron hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
ondansetron hydrochloride |
| Dosage Form: |
SOLUTION |
| Method: |
INTRAMUSCULAR; INTRAVENOUS |
| Original Marketing Date: |
30-08-2012 |
| Category Name: |
ANDA |
| Application Number: |
ANDA090648 |
| Labeler: |
SAGENT PHARMACEUTICALS |
| Substance Name: |
ONDANSETRON HYDROCHLORIDE |
| Active Numerator Strength: |
2 |
| Active Ingredient Unit: |
mg/mL |
| Pharm Classes: |
Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
| DEA Schedule: |
|
