Fentanyl - 52959-585-05 - (fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 52959-585
Proprietary Name: Fentanyl
Non Proprietary Name: fentanyl
Active Ingredient(s): 25    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: 52959-585
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077775
Marketing Category: ANDA
Start Marketing Date: 20100301

Package Information of Fentanyl

Package NDC: 52959-585-05
Package Description: 5 POUCH in 1 CARTON (52959-585-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 52959-585-05
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (52959-585-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Product NDC 52959-585
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20100301
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name FENTANYL
Strength Number 25
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information