Visitor Monitoring Drug Details: INNOPRAN XL
 
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Drug Details

Drug Name: INNOPRAN XL
FDA Application No: (NDA) 021438
Active Ingredient(s): PROPRANOLOL HYDROCHLORIDE
Company: RELIANT PHARMS
Original Approval or Tentative Approval Date: March 12, 2003
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
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
INNOPRAN XL PROPRANOLOL HYDROCHLORIDE80MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No BX
INNOPRAN XL PROPRANOLOL HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No BX


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