Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 072609
Company: WATSON LABS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PRAZOSIN HYDROCHLORIDE PRAZOSIN HYDROCHLORIDE EQ 5MG 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.

08/31/1990 SUPPL-4 Manufacturing (CMC)

Label is not available on this site.

06/29/1990 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

05/23/1990 SUPPL-2 Manufacturing (CMC)

Label is not available on this site.

03/13/1990 SUPPL-1 Labeling

Label is not available on this site.

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