Visitor Monitoring Drug Details: HYDROXYPROGESTERONE CAPROATE
 
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Drug Details

Drug Name: HYDROXYPROGESTERONE CAPROATE
FDA Application No: (NDA) 017439
Active Ingredient(s): HYDROXYPROGESTERONE CAPROATE
Company: WATSON LABS
Original Approval or Tentative Approval Date: October 3, 1975
Chemical Type: 5 New manufacturer
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
HYDROXYPROGESTERONE CAPROATE HYDROXYPROGESTERONE CAPROATE125MG/MLINJECTABLE; INJECTION Discontinued No None
HYDROXYPROGESTERONE CAPROATE HYDROXYPROGESTERONE CAPROATE250MG/MLINJECTABLE; INJECTION Discontinued No None


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