Fentanyl - 60760-914-05 - (FENTANYL)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 60760-914
Proprietary Name: Fentanyl
Non Proprietary Name: FENTANYL
Active Ingredient(s): 100    ug/h & nbsp;   FENTANYL
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 60760-914
Labeler Name: St. Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077062
Marketing Category: ANDA
Start Marketing Date: 20110126

Package Information of Fentanyl

Package NDC: 60760-914-05
Package Description: 5 POUCH in 1 CARTON (60760-914-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 60760-914-05
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (60760-914-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Product NDC 60760-914
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENTANYL
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20110126
Marketing Category Name ANDA
Labeler Name St. Marys Medical Park Pharmacy
Substance Name FENTANYL
Strength Number 100
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information