Fentanyl - 0245-0423-05 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 0245-0423
Proprietary Name: Fentanyl
Non Proprietary Name: Fentanyl
Active Ingredient(s): 100    ug/h & nbsp;   Fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 0245-0423
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077775
Marketing Category: ANDA
Start Marketing Date: 20130301

Package Information of Fentanyl

Package NDC: 0245-0423-05
Package Description: 5 POUCH in 1 CARTON (0245-0423-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH (0245-0423-89)

NDC Information of Fentanyl

NDC Code 0245-0423-05
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (0245-0423-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH (0245-0423-89)
Product NDC 0245-0423
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20130301
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
Substance Name FENTANYL
Strength Number 100
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information