ACTIQ - 63459-506-30 - (fentanyl citrate)

Alphabetical Index


Drug Information of ACTIQ

Product NDC: 63459-506
Proprietary Name: ACTIQ
Non Proprietary Name: fentanyl citrate
Active Ingredient(s): 600    ug/1 & nbsp;   fentanyl citrate
Administration Route(s): ORAL; TRANSMUCOSAL
Dosage Form(s): LOZENGE
Coding System: National Drug Codes(NDC)

Labeler Information of ACTIQ

Product NDC: 63459-506
Labeler Name: Cephalon, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020747
Marketing Category: NDA
Start Marketing Date: 19981104

Package Information of ACTIQ

Package NDC: 63459-506-30
Package Description: 10 BLISTER PACK in 1 CARTON (63459-506-30) > 3 LOZENGE in 1 BLISTER PACK (63459-506-01)

NDC Information of ACTIQ

NDC Code 63459-506-30
Proprietary Name ACTIQ
Package Description 10 BLISTER PACK in 1 CARTON (63459-506-30) > 3 LOZENGE in 1 BLISTER PACK (63459-506-01)
Product NDC 63459-506
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl citrate
Dosage Form Name LOZENGE
Route Name ORAL; TRANSMUCOSAL
Start Marketing Date 19981104
Marketing Category Name NDA
Labeler Name Cephalon, Inc.
Substance Name FENTANYL CITRATE
Strength Number 600
Strength Unit ug/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of ACTIQ


General Information