Visitor Monitoring Drug Details: EDEX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: EDEX
FDA Application No: (NDA) 020649
Active Ingredient(s): ALPROSTADIL
Company: SCHWARZ PHARMA
Original Approval or Tentative Approval Date: June 12, 1997
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
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
EDEX ALPROSTADIL0.005MG/VIALINJECTABLE; INJECTION Discontinued No None
EDEX ALPROSTADIL0.01MG/VIALINJECTABLE; INJECTION Prescription No AP
EDEX ALPROSTADIL0.02MG/VIALINJECTABLE; INJECTION Prescription No AP
EDEX ALPROSTADIL0.04MG/VIALINJECTABLE; INJECTION Prescription Yes AP
EDEX ALPROSTADIL0.01MG/VIALINJECTABLE; INJECTION Prescription Yes None
EDEX ALPROSTADIL0.02MG/VIALINJECTABLE; INJECTION Prescription Yes None
EDEX ALPROSTADIL0.04MG/VIALINJECTABLE; INJECTION Prescription Yes None


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