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Buprenorphine hydrochloride and naloxone hydrochloride dihydrate - 0228-3154-03 - (Buprenorphine hydrochloride and naloxone hydrochloride dihydrate)

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Drug Information of Buprenorphine hydrochloride and naloxone hydrochloride dihydrate

Product NDC: 0228-3154
Proprietary Name: Buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Non Proprietary Name: Buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Active Ingredient(s): 2; .5    mg/1; mg/1 & nbsp;   Buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Administration Route(s): SUBLINGUAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Buprenorphine hydrochloride and naloxone hydrochloride dihydrate

Product NDC: 0228-3154
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091422
Marketing Category: ANDA
Start Marketing Date: 20130304

Package Information of Buprenorphine hydrochloride and naloxone hydrochloride dihydrate

Package NDC: 0228-3154-03
Package Description: 30 TABLET in 1 BOTTLE (0228-3154-03)

NDC Information of Buprenorphine hydrochloride and naloxone hydrochloride dihydrate

NDC Code 0228-3154-03
Proprietary Name Buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Package Description 30 TABLET in 1 BOTTLE (0228-3154-03)
Product NDC 0228-3154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Dosage Form Name TABLET
Route Name SUBLINGUAL
Start Marketing Date 20130304
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name BUPRENORPHINE; NALOXONE
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 Buprenorphine hydrochloride and naloxone hydrochloride dihydrate


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