Fentanyl - 67253-942-55 - (fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 67253-942
Proprietary Name: Fentanyl
Non Proprietary Name: fentanyl
Active Ingredient(s): 75    ug/h & nbsp;   fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 67253-942
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077051
Marketing Category: ANDA
Start Marketing Date: 20101101

Package Information of Fentanyl

Package NDC: 67253-942-55
Package Description: 5 POUCH in 1 CARTON (67253-942-55) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 67253-942-55
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (67253-942-55) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Product NDC 67253-942
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20101101
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
Substance Name FENTANYL
Strength Number 75
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information