Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 072352
Company: WATSON LABS
Company: WATSON LABS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
PRAZOSIN HYDROCHLORIDE | PRAZOSIN HYDROCHLORIDE | EQ 1MG BASE | CAPSULE;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 |
---|---|---|---|---|---|---|---|
01/11/1989 | 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 |
---|---|---|---|---|---|
01/28/1991 | SUPPL-6 | Manufacturing (CMC) |
Label is not available on this site. |
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08/31/1990 | SUPPL-4 | Manufacturing (CMC) |
Label is not available on this site. |
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06/29/1990 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |
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05/24/1990 | SUPPL-2 | Manufacturing (CMC) |
Label is not available on this site. |
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05/24/1990 | SUPPL-1 | Labeling |
Label is not available on this site. |