Home > National Drug Code (NDC) > Fentanyl - NOVAPLUS

Fentanyl - NOVAPLUS - 0591-3601-72 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl - NOVAPLUS

Product NDC: 0591-3601
Proprietary Name: Fentanyl - NOVAPLUS
Non Proprietary Name: Fentanyl
Active Ingredient(s): 50    ug/h & nbsp;   Fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl - NOVAPLUS

Product NDC: 0591-3601
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076709
Marketing Category: ANDA
Start Marketing Date: 20070901

Package Information of Fentanyl - NOVAPLUS

Package NDC: 0591-3601-72
Package Description: 5 POUCH in 1 CARTON (0591-3601-72) > 1 PATCH in 1 POUCH (0591-3601-54) > 72 h in 1 PATCH

NDC Information of Fentanyl - NOVAPLUS

NDC Code 0591-3601-72
Proprietary Name Fentanyl - NOVAPLUS
Package Description 5 POUCH in 1 CARTON (0591-3601-72) > 1 PATCH in 1 POUCH (0591-3601-54) > 72 h in 1 PATCH
Product NDC 0591-3601
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 Watson Laboratories, Inc.
Substance Name FENTANYL
Strength Number 50
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl - NOVAPLUS


General Information