Fentanyl - 60505-7002-2 - (fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 60505-7002
Proprietary Name: Fentanyl
Non Proprietary Name: fentanyl
Active Ingredient(s): 50    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: 60505-7002
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077775
Marketing Category: ANDA
Start Marketing Date: 20100301

Package Information of Fentanyl

Package NDC: 60505-7002-2
Package Description: 5 POUCH in 1 CARTON (60505-7002-2) > 1 PATCH in 1 POUCH (60505-7002-0) > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 60505-7002-2
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (60505-7002-2) > 1 PATCH in 1 POUCH (60505-7002-0) > 72 h in 1 PATCH
Product NDC 60505-7002
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 Apotex Corp.
Substance Name FENTANYL
Strength Number 50
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information