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Buprenorphine hydrochloride - 63629-4092-1 - (Buprenorphine hydrochloride)

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Drug Information of Buprenorphine hydrochloride

Product NDC: 63629-4092
Proprietary Name: Buprenorphine hydrochloride
Non Proprietary Name: Buprenorphine hydrochloride
Active Ingredient(s): 8    mg/1 & nbsp;   Buprenorphine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Buprenorphine hydrochloride

Product NDC: 63629-4092
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA020732
Marketing Category: ANDA
Start Marketing Date: 20091009

Package Information of Buprenorphine hydrochloride

Package NDC: 63629-4092-1
Package Description: 10 TABLET in 1 BOTTLE (63629-4092-1)

NDC Information of Buprenorphine hydrochloride

NDC Code 63629-4092-1
Proprietary Name Buprenorphine hydrochloride
Package Description 10 TABLET in 1 BOTTLE (63629-4092-1)
Product NDC 63629-4092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buprenorphine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091009
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
Substance Name BUPRENORPHINE HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA]

Complete Information of Buprenorphine hydrochloride


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