Butrans - 35356-606-04 - (buprenorphine)

Alphabetical Index


Drug Information of Butrans

Product NDC: 35356-606
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: 35356-606
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021306
Marketing Category: NDA
Start Marketing Date: 20120326

Package Information of Butrans

Package NDC: 35356-606-04
Package Description: 4 POUCH in 1 CARTON (35356-606-04) > 1 PATCH in 1 POUCH > 168 h in 1 PATCH

NDC Information of Butrans

NDC Code 35356-606-04
Proprietary Name Butrans
Package Description 4 POUCH in 1 CARTON (35356-606-04) > 1 PATCH in 1 POUCH > 168 h in 1 PATCH
Product NDC 35356-606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name buprenorphine
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20120326
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products 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