| NDC Code: |
60505-3718 |
| Proprietary Name: |
Zolmitriptan |
| Suffix: |
|
| Non-Proprietary Name: |
Zolmitriptan |
| Dosage Form: |
TABLET, ORALLY DISINTEGRATING |
| Method: |
ORAL |
| Original Marketing Date: |
14-05-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA202476 |
| Labeler: |
APOTEX CORP |
| Substance Name: |
ZOLMITRIPTAN |
| Active Numerator Strength: |
2.5 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
| DEA Schedule: |
|
