Abstral - 42747-221-32 - (fentanyl)

Alphabetical Index


Drug Information of Abstral

Product NDC: 42747-221
Proprietary Name: Abstral
Non Proprietary Name: fentanyl
Active Ingredient(s): 100    ug/1 & nbsp;   fentanyl
Administration Route(s): SUBLINGUAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Abstral

Product NDC: 42747-221
Labeler Name: ProStrakan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022510
Marketing Category: NDA
Start Marketing Date: 20110107

Package Information of Abstral

Package NDC: 42747-221-32
Package Description: 32 TABLET in 1 BLISTER PACK (42747-221-32)

NDC Information of Abstral

NDC Code 42747-221-32
Proprietary Name Abstral
Package Description 32 TABLET in 1 BLISTER PACK (42747-221-32)
Product NDC 42747-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fentanyl
Dosage Form Name TABLET
Route Name SUBLINGUAL
Start Marketing Date 20110107
Marketing Category Name NDA
Labeler Name ProStrakan, Inc.
Substance Name FENTANYL CITRATE
Strength Number 100
Strength Unit ug/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Abstral


General Information