Fentanyl - 63629-4982-3 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 63629-4982
Proprietary Name: Fentanyl
Non Proprietary Name: Fentanyl
Active Ingredient(s): 75    ug/h & nbsp;   Fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 63629-4982
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076709
Marketing Category: ANDA
Start Marketing Date: 20070901

Package Information of Fentanyl

Package NDC: 63629-4982-3
Package Description: 5 h in 1 BOTTLE (63629-4982-3)

NDC Information of Fentanyl

NDC Code 63629-4982-3
Proprietary Name Fentanyl
Package Description 5 h in 1 BOTTLE (63629-4982-3)
Product NDC 63629-4982
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20070901
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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