Fentanyl - 54868-0244-0 - (fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 54868-0244
Proprietary Name: Fentanyl
Non Proprietary Name: fentanyl
Active Ingredient(s): 5.1    mg/[USP'U] & nbsp;   fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 54868-0244
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076258
Marketing Category: ANDA
Start Marketing Date: 20050714

Package Information of Fentanyl

Package NDC: 54868-0244-0
Package Description: 5 POUCH in 1 CARTON (54868-0244-0) > 1 PATCH in 1 POUCH > 72 [USP'U] in 1 PATCH

NDC Information of Fentanyl

NDC Code 54868-0244-0
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (54868-0244-0) > 1 PATCH in 1 POUCH > 72 [USP'U] in 1 PATCH
Product NDC 54868-0244
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20050714
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name FENTANYL
Strength Number 5.1
Strength Unit mg/[USP'U]
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information