Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 200884
Company: SUN PHARM
Company: SUN PHARM
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| FENOFIBRATE | FENOFIBRATE | 48MG | TABLET;ORAL | Discontinued | None | No | No |
| FENOFIBRATE | FENOFIBRATE | 145MG | TABLET;ORAL | Discontinued | None | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 09/07/2017 | ORIG-1 | Approval | Not Applicable |
Label is not available on this site. |