Visitor Monitoring Drug Details: RETROVIR
 
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Drug Details

Drug Name: RETROVIR
FDA Application No: (NDA) 020518
Active Ingredient(s): ZIDOVUDINE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: December 19, 1995
Chemical Type: 3 New dosage form
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
RETROVIR ZIDOVUDINE200MGTABLET; ORAL Discontinued No None
RETROVIR ZIDOVUDINE300MGTABLET; ORAL Prescription Yes AB


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