Fentanyl - 0093-6901-45 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 0093-6901
Proprietary Name: Fentanyl
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

Product NDC: 0093-6901
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077449
Marketing Category: ANDA
Start Marketing Date: 20081222

Package Information of Fentanyl

Package NDC: 0093-6901-45
Package Description: 5 BLISTER PACK in 1 CARTON (0093-6901-45) > 1 PATCH in 1 BLISTER PACK (0093-6901-19) > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 0093-6901-45
Proprietary Name Fentanyl
Package Description 5 BLISTER PACK in 1 CARTON (0093-6901-45) > 1 PATCH in 1 BLISTER PACK (0093-6901-19) > 72 h in 1 PATCH
Product NDC 0093-6901
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20081222
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FENTANYL
Strength Number 50
Strength Unit ug/h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information