Visitor Monitoring Drug Details: ALTACE
 
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Drug Details

Drug Name: ALTACE
FDA Application No: (NDA) 019901
Active Ingredient(s): RAMIPRIL
Company: KING PHARMS
Original Approval or Tentative Approval Date: January 28, 1991
Chemical Type: 1 New molecular entity (NME)
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
ALTACE RAMIPRIL1.25MGCAPSULE; ORAL Prescription No None
ALTACE RAMIPRIL2.5MGCAPSULE; ORAL Prescription No None
ALTACE RAMIPRIL5MGCAPSULE; ORAL Prescription No None
ALTACE RAMIPRIL10MGCAPSULE; ORAL Prescription Yes None


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