Ondansetron Hydrochloride - Ondansetron Hydrochloride
Navigation: NDC > Supplier starting with: A > AUROBINDO PHARMA LIMITED| Field | Value |
|---|---|
| NDC Code: | 65862-188 |
| Proprietary Name: | Ondansetron Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Ondansetron Hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 31-07-2007 |
| Category Name: | ANDA |
| Application Number: | ANDA078539 |
| Labeler: | AUROBINDO PHARMA LIMITED |
| Substance Name: | ONDANSETRON HYDROCHLORIDE |
| Active Numerator Strength: | 8 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
| DEA Schedule: |