Visitor Monitoring Drug Details: ACTIQ
 
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Drug Details

Drug Name: ACTIQ
FDA Application No: (NDA) 020747
Active Ingredient(s): FENTANYL CITRATE
Company: CEPHALON
Original Approval or Tentative Approval Date: November 4, 1998
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
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ACTIQ FENTANYL CITRATEEQ 0.2MG BASETROCHE/LOZENGE; TRANSMUCOSAL Prescription No None
ACTIQ FENTANYL CITRATEEQ 0.4MG BASETROCHE/LOZENGE; TRANSMUCOSAL Prescription Yes None
ACTIQ FENTANYL CITRATEEQ 0.6MG BASETROCHE/LOZENGE; TRANSMUCOSAL Prescription No None
ACTIQ FENTANYL CITRATEEQ 0.8MG BASETROCHE/LOZENGE; TRANSMUCOSAL Prescription No None
ACTIQ FENTANYL CITRATEEQ 1.2MG BASETROCHE/LOZENGE; TRANSMUCOSAL Prescription No None
ACTIQ FENTANYL CITRATEEQ 1.6MG BASETROCHE/LOZENGE; TRANSMUCOSAL Prescription No None


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