Fentanyl - 0378-9119-98 - (fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 0378-9119
Proprietary Name: Fentanyl
Non Proprietary Name: fentanyl
Active Ingredient(s): 12    ug/h & nbsp;   fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 0378-9119
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076258
Marketing Category: ANDA
Start Marketing Date: 20130109

Package Information of Fentanyl

Package NDC: 0378-9119-98
Package Description: 5 POUCH in 1 CARTON (0378-9119-98) > 1 PATCH in 1 POUCH (0378-9119-16) > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 0378-9119-98
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (0378-9119-98) > 1 PATCH in 1 POUCH (0378-9119-16) > 72 h in 1 PATCH
Product NDC 0378-9119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20130109
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name FENTANYL
Strength Number 12
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information