Visitor Monitoring Drug Details: FENTANYL
 
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Drug Details

Drug Name: FENTANYL
FDA Application No: (NDA) 020195
Active Ingredient(s): FENTANYL CITRATE
Company: CEPHALON
Original Approval or Tentative Approval Date: October 4, 1993
Chemical Type: 3 New dosage form
Review Classification: P Priority review drug
 
 
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
FENTANYL FENTANYL CITRATEEQ 0.2MG BASETROCHE/LOZENGE; ORAL Discontinued No None
FENTANYL FENTANYL CITRATEEQ 0.3MG BASETROCHE/LOZENGE; ORAL Discontinued No None
FENTANYL FENTANYL CITRATEEQ 0.4MG BASETROCHE/LOZENGE; ORAL Discontinued No None
FENTANYL FENTANYL CITRATEEQ 0.1MG BASETROCHE/LOZENGE; ORAL Discontinued No None


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