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FENTANYL TRANSDERMAL SYSTEM - 63629-4771-1 - (fentanyl transdermal system)

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Drug Information of FENTANYL TRANSDERMAL SYSTEM

Product NDC: 63629-4771
Proprietary Name: FENTANYL TRANSDERMAL SYSTEM
Non Proprietary Name: fentanyl transdermal system
Active Ingredient(s): 50    ug/h & nbsp;   fentanyl transdermal system
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of FENTANYL TRANSDERMAL SYSTEM

Product NDC: 63629-4771
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077154
Marketing Category: ANDA
Start Marketing Date: 20110606

Package Information of FENTANYL TRANSDERMAL SYSTEM

Package NDC: 63629-4771-1
Package Description: 1 h in 1 BOTTLE (63629-4771-1)

NDC Information of FENTANYL TRANSDERMAL SYSTEM

NDC Code 63629-4771-1
Proprietary Name FENTANYL TRANSDERMAL SYSTEM
Package Description 1 h in 1 BOTTLE (63629-4771-1)
Product NDC 63629-4771
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl transdermal system
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20110606
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name FENTANYL
Strength Number 50
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of FENTANYL TRANSDERMAL SYSTEM


General Information