Visitor Monitoring Drug Details: MORPHINE SULFATE
 
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Drug Details

Drug Name: MORPHINE SULFATE
FDA Application No: (ANDA) 074862
Active Ingredient(s): MORPHINE SULFATE
Company: AB GENERICS
Original Approval or Tentative Approval Date: July 7, 1998
 
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
MORPHINE SULFATE MORPHINE SULFATE15MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
MORPHINE SULFATE MORPHINE SULFATE30MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
MORPHINE SULFATE MORPHINE SULFATE60MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB


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