Visitor Monitoring Drug Details: DEPO-PROVERA
 
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Drug Details

Drug Name: DEPO-PROVERA
FDA Application No: (NDA) 012541
Active Ingredient(s): MEDROXYPROGESTERONE ACETATE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: September 23, 1960
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no 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
DEPO-PROVERA MEDROXYPROGESTERONE ACETATE100MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None
DEPO-PROVERA MEDROXYPROGESTERONE ACETATE400MG/MLINJECTABLE; INJECTION Prescription Yes None


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