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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 018031
Company: WYETH PHARMS INC

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
INDERIDE-40/25 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE 25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET;ORAL Discontinued None Yes No
INDERIDE-80/25 HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE 25MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET;ORAL Discontinued None Yes No

Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert		 Note Url
03/17/2011 SUPPL-38 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/018031s037s038lbl.pdf
03/17/2011 SUPPL-37 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2011/018031s037s038lbl.pdf
03/04/2010 SUPPL-36 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/018031s036lbl.pdf
01/02/2008 SUPPL-35 Labeling Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/018031s035lbl.pdf
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