Suboxone - 63629-4028-2 - (buprenorphine and naloxone)

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Drug Information of Suboxone

Product NDC: 63629-4028
Proprietary Name: Suboxone
Non Proprietary Name: buprenorphine and naloxone
Active Ingredient(s): 2; .5    mg/1; mg/1 & nbsp;   buprenorphine and naloxone
Administration Route(s): SUBLINGUAL
Dosage Form(s): FILM, SOLUBLE
Coding System: National Drug Codes(NDC)

Labeler Information of Suboxone

Product NDC: 63629-4028
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022410
Marketing Category: NDA
Start Marketing Date: 20100913

Package Information of Suboxone

Package NDC: 63629-4028-2
Package Description: 30 FILM, SOLUBLE in 1 BOTTLE (63629-4028-2)

NDC Information of Suboxone

NDC Code 63629-4028-2
Proprietary Name Suboxone
Package Description 30 FILM, SOLUBLE in 1 BOTTLE (63629-4028-2)
Product NDC 63629-4028
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name buprenorphine and naloxone
Dosage Form Name FILM, SOLUBLE
Route Name SUBLINGUAL
Start Marketing Date 20100913
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Strength Number 2; .5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA]

Complete Information of Suboxone


General Information