Suboxone
Active Ingredient(s): Buprenorphine First Approved by the FDA: October 8, 2002 Pharmaceutical Company: RECKITT BENCKISER
Suboxone Article Summary
Buprenorphine Is A Semi-synthetic Opiate With Partial Agonist And Antagonist Actions. Buprenorphine Hydrochloride Was First Marketed In The 1980s By Reckitt & Colman (now Reckitt Benckiser) As An Analgesic, Available Generally As Temgesic 0.2 mg Sublingual Tablets, And As Buprenex In A 0.3 mg/ml Injectable Formulation. In October 2002, The Food And Drug Administration (fda) Of The United States Of America Additionally Approved Suboxone And Subutex, Buprenorphine's High-dose Subling
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This article is from Wikipedia. All text is available under the terms of the GFDL
(GNU Free Documentation License) | http://en.wikipedia.org/wiki/Suboxone
Possible Dosages for this and Related Drugs:
Note: May Include Dosages for Drugs similar to Suboxone
Injection
0.3mg/ml
Tablet
2mg,
2mg + 0.5mg,
8mg,
8mg + 2mg
Related Drug Page(s):
Buprenex Buprenorphine
Buprenorphine
Subutex Buprenorphine
Related Search Results for Suboxone
Possibly Related Topicssuboxone and adderallsuboxone 8mg/2mg and roxy 30'ssuboxone 8mg/2mg orange octagonsuboxone painsuboxone doctorssuboxone/personality changesuboxone side effectssuboxone withdrawalsuboxone and somasuboxone providers
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Drugs/Suboxone.asp Last Updated October 28 2009
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