Drugs@FDA: FDA Approved Drug Products

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Abbreviated New Drug Application (ANDA): 083383
Company: WYETH AYERST
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DIUCARDIN HYDROFLUMETHIAZIDE 50MG 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
12/20/1973 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
12/28/1990 SUPPL-14 Labeling

Label is not available on this site.

12/28/1990 SUPPL-13 Labeling

Label is not available on this site.

01/18/1989 SUPPL-12 Labeling

Label is not available on this site.

12/28/1987 SUPPL-11 Manufacturing (CMC)

Label is not available on this site.

07/12/1982 SUPPL-9 Manufacturing (CMC)

Label is not available on this site.

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