Visitor Monitoring Drug Details: NATURETIN-10
 
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Drug Details

Drug Name: NATURETIN-10
FDA Application No: (NDA) 012164
Active Ingredient(s): BENDROFLUMETHIAZIDE
Company: APOTHECON
Original Approval or Tentative Approval Date: December 7, 1959
Chemical Type: 3 New dosage form
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
NATURETIN-10 BENDROFLUMETHIAZIDE10MGTABLET; ORAL Discontinued No None
NATURETIN-2.5 BENDROFLUMETHIAZIDE2.5MGTABLET; ORAL Discontinued No None
NATURETIN-5 BENDROFLUMETHIAZIDE5MGTABLET; ORAL Discontinued No None


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