Visitor Monitoring Drug Details: ORETIC
 
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Drug Details

Drug Name: ORETIC
FDA Application No: (NDA) 011971
Active Ingredient(s): HYDROCHLOROTHIAZIDE
Company: ABBOTT
Original Approval or Tentative Approval Date: July 6, 1959
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ORETIC HYDROCHLOROTHIAZIDE25MGTABLET; ORAL Discontinued No None
ORETIC HYDROCHLOROTHIAZIDE50MGTABLET; ORAL Prescription No AB


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