Butrans

Active Ingredient(s): Buprenorphine
FDA Approved: * June 30, 2010
Pharm Company: * PURDUE PHARMA LP
Category: Opioid Dependence

Buprenorphine/naloxone, sold under the brand name Suboxone among others, is a fixed-dose combination medication that includes buprenorphine and naloxone.[2] It is used to treat opioid use disorder, and reduces the mortality of opioid use disorder by 50% (namely by reducing the risk of overdose on full-agonist opioids such as heroin or fentanyl).[2][4][5] It relieves cravings to use and withdrawal symptoms.[6] Bupr... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
57 Discussions

Dosage List

Butrans 10 ug/H Transdermal Patch, Extended Release
NDC: 35356-605
Labeler:
Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
Butrans 20 ug/H Transdermal Patch, Extended Release
NDC: 35356-606
Labeler:
Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
Butrans 5 ug/H Transdermal Patch, Extended Release
NDC: 35356-607
Labeler:
Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
Butrans 10 ug/H Transdermal Patch, Extended Release
NDC: 54569-6325
Labeler:
A-s Medication Solutions LLC
Butrans 20 ug/H Transdermal Patch, Extended Release
NDC: 54569-6326
Labeler:
A-s Medication Solutions LLC
Butrans 5 ug/H Transdermal Patch, Extended Release
NDC: 59011-750
Labeler:
Purdue Pharma Lp
Butrans 10 ug/H Transdermal Patch, Extended Release
NDC: 59011-751
Labeler:
Purdue Pharma Lp
Butrans 20 ug/H Transdermal Patch, Extended Release
NDC: 59011-752
Labeler:
Purdue Pharma Lp
Butrans 7.5 ug/H Transdermal Patch, Extended Release
NDC: 59011-757
Labeler:
Purdue Pharma Lp
Butrans 15 ug/H Transdermal Patch, Extended Release
NDC: 59011-758
Labeler:
Purdue Pharma Lp

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