Fentanyl - 68258-3023-1 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 68258-3023
Proprietary Name: Fentanyl
Non Proprietary Name: Fentanyl
Active Ingredient(s): 25    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: 68258-3023
Labeler Name: Dispensing Solutions Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077449
Marketing Category: ANDA
Start Marketing Date: 20061106

Package Information of Fentanyl

Package NDC: 68258-3023-1
Package Description: 5 PATCH in 1 CARTON (68258-3023-1) > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 68258-3023-1
Proprietary Name Fentanyl
Package Description 5 PATCH in 1 CARTON (68258-3023-1) > 72 h in 1 PATCH
Product NDC 68258-3023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20061106
Marketing Category Name ANDA
Labeler Name Dispensing Solutions Inc.
Substance Name FENTANYL
Strength Number 25
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information