suboxone - 63629-4034-2 - (buprenorphine hydrochloride and naloxone hydrochloride)

Alphabetical Index


Drug Information of suboxone

Product NDC: 63629-4034
Proprietary Name: suboxone
Non Proprietary Name: buprenorphine hydrochloride and naloxone hydrochloride
Active Ingredient(s): 8; 2    mg/1; mg/1 & nbsp;   buprenorphine hydrochloride and naloxone hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of suboxone

Product NDC: 63629-4034
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020733
Marketing Category: NDA
Start Marketing Date: 20090723

Package Information of suboxone

Package NDC: 63629-4034-2
Package Description: 10 TABLET in 1 BOTTLE (63629-4034-2)

NDC Information of suboxone

NDC Code 63629-4034-2
Proprietary Name suboxone
Package Description 10 TABLET in 1 BOTTLE (63629-4034-2)
Product NDC 63629-4034
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name buprenorphine hydrochloride and naloxone hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090723
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Strength Number 8; 2
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