Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 200149
Company: ACTAVIS GRP PTC
Company: ACTAVIS GRP PTC
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
SILDENAFIL CITRATE | SILDENAFIL CITRATE | EQ 20MG BASE | 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 |
---|---|---|---|---|---|---|---|
02/25/2013 | ORIG-1 | Approval | Not Applicable |
Label is not available on this site. |