Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 086348
Company: WYETH AYERST
Company: WYETH AYERST
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| PROCHLORPERAZINE EDISYLATE | PROCHLORPERAZINE EDISYLATE | EQ 5MG BASE/ML | INJECTABLE;INJECTION | 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 |
|---|---|---|---|---|---|---|---|
| 07/05/1979 | ORIG-1 | Approval |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 04/27/1989 | SUPPL-9 | Labeling |
Label is not available on this site. |
||
| 08/27/1986 | SUPPL-7 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 11/29/1984 | SUPPL-5 | Manufacturing (CMC) |
Label is not available on this site. |
||
| 05/01/1987 | SUPPL-2 | Manufacturing (CMC) |
Label is not available on this site. |