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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 089530
Company: WATSON LABS
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
07/08/1987 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
02/23/2017 SUPPL-14 Labeling-Package Insert

Label is not available on this site.

11/03/2015 SUPPL-13 Labeling-Package Insert

Label is not available on this site.

02/19/1999 SUPPL-10 Manufacturing (CMC)-Microbiology-Processing

Label is not available on this site.

02/02/1999 SUPPL-9 Manufacturing (CMC)-Microbiology-Processing

Label is not available on this site.

12/04/1996 SUPPL-8 Manufacturing (CMC)-Microbiology-Processing

Label is not available on this site.

10/19/1993 SUPPL-7 Labeling

Label is not available on this site.

05/11/1992 SUPPL-6 Labeling

Label is not available on this site.

08/12/1991 SUPPL-5 Labeling

Label is not available on this site.

03/20/1991 SUPPL-4 Labeling

Label is not available on this site.

04/18/1989 SUPPL-3 Manufacturing (CMC)

Label is not available on this site.

06/02/1988 SUPPL-1 Labeling

Label is not available on this site.

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