FENTORA - 63459-546-28 - (fentanyl citrate)

Alphabetical Index


Drug Information of FENTORA

Product NDC: 63459-546
Proprietary Name: FENTORA
Non Proprietary Name: fentanyl citrate
Active Ingredient(s): 600    ug/1 & nbsp;   fentanyl citrate
Administration Route(s): BUCCAL; ORAL; TRANSMUCOSAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FENTORA

Product NDC: 63459-546
Labeler Name: Cephalon, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021947
Marketing Category: NDA
Start Marketing Date: 20060925

Package Information of FENTORA

Package NDC: 63459-546-28
Package Description: 7 BLISTER PACK in 1 CARTON (63459-546-28) > 4 TABLET in 1 BLISTER PACK (63459-546-04)

NDC Information of FENTORA

NDC Code 63459-546-28
Proprietary Name FENTORA
Package Description 7 BLISTER PACK in 1 CARTON (63459-546-28) > 4 TABLET in 1 BLISTER PACK (63459-546-04)
Product NDC 63459-546
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl citrate
Dosage Form Name TABLET
Route Name BUCCAL; ORAL; TRANSMUCOSAL
Start Marketing Date 20060925
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 FENTORA


General Information