SUBSYS - 20482-001-10 - (FENTANYL)

Alphabetical Index


Drug Information of SUBSYS

Product NDC: 20482-001
Proprietary Name: SUBSYS
Non Proprietary Name: FENTANYL
Active Ingredient(s): .1    mg/1 & nbsp;   FENTANYL
Administration Route(s): SUBLINGUAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of SUBSYS

Product NDC: 20482-001
Labeler Name: Insys Therapeutics, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202788
Marketing Category: NDA
Start Marketing Date: 20120313

Package Information of SUBSYS

Package NDC: 20482-001-10
Package Description: 10 BLISTER PACK in 1 CARTON (20482-001-10) > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 1 SPRAY in 1 BOTTLE, SPRAY

NDC Information of SUBSYS

NDC Code 20482-001-10
Proprietary Name SUBSYS
Package Description 10 BLISTER PACK in 1 CARTON (20482-001-10) > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 1 SPRAY in 1 BOTTLE, SPRAY
Product NDC 20482-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FENTANYL
Dosage Form Name SPRAY
Route Name SUBLINGUAL
Start Marketing Date 20120313
Marketing Category Name NDA
Labeler Name Insys Therapeutics, Inc.
Substance Name FENTANYL
Strength Number .1
Strength Unit mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of SUBSYS


General Information