Butrans - 54569-6326-0 - (buprenorphine)

Alphabetical Index


Drug Information of Butrans

Product NDC: 54569-6326
Proprietary Name: Butrans
Non Proprietary Name: buprenorphine
Active Ingredient(s): 20    ug/h & nbsp;   buprenorphine
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Butrans

Product NDC: 54569-6326
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021306
Marketing Category: NDA
Start Marketing Date: 20110214

Package Information of Butrans

Package NDC: 54569-6326-0
Package Description: 4 POUCH in 1 CARTON (54569-6326-0) > 1 PATCH in 1 POUCH > 168 h in 1 PATCH

NDC Information of Butrans

NDC Code 54569-6326-0
Proprietary Name Butrans
Package Description 4 POUCH in 1 CARTON (54569-6326-0) > 1 PATCH in 1 POUCH > 168 h in 1 PATCH
Product NDC 54569-6326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name buprenorphine
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20110214
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
Substance Name BUPRENORPHINE
Strength Number 20
Strength Unit ug/h
Pharmaceutical Classes Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA]

Complete Information of Butrans


General Information