Visitor Monitoring Drug Details: AMARYL
 
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Drug Details

Drug Name: AMARYL
FDA Application No: (NDA) 020496
Active Ingredient(s): GLIMEPIRIDE
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: November 30, 1995
Chemical Type: 1 New molecular entity (NME)
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
AMARYL GLIMEPIRIDE1MGTABLET; ORAL Prescription Yes AB
AMARYL GLIMEPIRIDE2MGTABLET; ORAL Prescription No AB
AMARYL GLIMEPIRIDE4MGTABLET; ORAL Prescription No AB


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