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
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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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