Fentanyl - 49999-833-05 - (Fentanyl)

Alphabetical Index


Drug Information of Fentanyl

Product NDC: 49999-833
Proprietary Name: Fentanyl
Non Proprietary Name: Fentanyl
Active Ingredient(s): 7.5    mg/72h & nbsp;   Fentanyl
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl

Product NDC: 49999-833
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076709
Marketing Category: ANDA
Start Marketing Date: 20111209

Package Information of Fentanyl

Package NDC: 49999-833-05
Package Description: 5 POUCH in 1 CARTON (49999-833-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH

NDC Information of Fentanyl

NDC Code 49999-833-05
Proprietary Name Fentanyl
Package Description 5 POUCH in 1 CARTON (49999-833-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH
Product NDC 49999-833
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20111209
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name FENTANYL
Strength Number 7.5
Strength Unit mg/72h
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl


General Information