DURAGESIC - 50458-091-05 - (fentanyl)

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Drug Information of DURAGESIC

Product NDC: 50458-091
Proprietary Name: DURAGESIC
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 DURAGESIC

Product NDC: 50458-091
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019813
Marketing Category: NDA
Start Marketing Date: 19900807

Package Information of DURAGESIC

Package NDC: 50458-091-05
Package Description: 5 POUCH in 1 BOX (50458-091-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH

NDC Information of DURAGESIC

NDC Code 50458-091-05
Proprietary Name DURAGESIC
Package Description 5 POUCH in 1 BOX (50458-091-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Product NDC 50458-091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 19900807
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name FENTANYL
Strength Number 25
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of DURAGESIC


General Information