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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 090150
Company: APOTEX
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5MG;50MG TABLET;ORAL Discontinued None No No
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 12.5MG;100MG TABLET;ORAL Discontinued None No No
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM 25MG;100MG 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
10/06/2010 ORIG-2 Approval

Label is not available on this site.

08/11/2010 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
02/24/2017 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

05/01/2015 SUPPL-9 Labeling-Package Insert

Label is not available on this site.

05/01/2015 SUPPL-8 Labeling-Package Insert

Label is not available on this site.

05/01/2015 SUPPL-7 Labeling-Package Insert

Label is not available on this site.

05/01/2015 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

11/05/2015 SUPPL-4 Labeling-Patient Package Insert, Labeling-Container/Carton Labels, Labeling-Package Insert

Label is not available on this site.

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