Fentanyl - 0781-7241-55 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 0781-7241
Proprietary Name: Fentanyl
Non Proprietary Name: Fentanyl
Active Ingredient(s): 25    ug/h & nbsp;   Fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 0781-7241
Labeler Name: Sandoz,Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019813
Marketing Category: NDA
Start Marketing Date: 20041001

Package Information of Fentanyl

Package NDC: 0781-7241-55
Package Description: 5 POUCH in 1 BOX (0781-7241-55) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 0781-7241-55
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 BOX (0781-7241-55) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Product NDC 0781-7241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20041001
Marketing Category Name NDA
Labeler Name Sandoz,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