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
 
There are no 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
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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