Visitor Monitoring Drug Details: RAMIPRIL
 
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Drug Details

Drug Name: RAMIPRIL
FDA Application No: (ANDA) 078191
Active Ingredient(s): RAMIPRIL
Company: DR REDDYS LABS LTD
Original Approval or Tentative Approval Date: August 13, 2007
 
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
RAMIPRIL RAMIPRIL1.25MGCAPSULE; ORAL Tentative Approval No None
RAMIPRIL RAMIPRIL2.5MGCAPSULE; ORAL Tentative Approval No None
RAMIPRIL RAMIPRIL5MGCAPSULE; ORAL Tentative Approval No None
RAMIPRIL RAMIPRIL10MGCAPSULE; ORAL Tentative Approval No None


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