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Buprenorphine Hydrochloride - 0093-5378-56 - (Buprenorphine Hydrochloride)

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Drug Information of Buprenorphine Hydrochloride

Product NDC: 0093-5378
Proprietary Name: Buprenorphine Hydrochloride
Non Proprietary Name: Buprenorphine Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Buprenorphine Hydrochloride
Administration Route(s): SUBLINGUAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Buprenorphine Hydrochloride

Product NDC: 0093-5378
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090360
Marketing Category: ANDA
Start Marketing Date: 20100525

Package Information of Buprenorphine Hydrochloride

Package NDC: 0093-5378-56
Package Description: 30 TABLET in 1 BOTTLE (0093-5378-56)

NDC Information of Buprenorphine Hydrochloride

NDC Code 0093-5378-56
Proprietary Name Buprenorphine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (0093-5378-56)
Product NDC 0093-5378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Buprenorphine Hydrochloride
Dosage Form Name TABLET
Route Name SUBLINGUAL
Start Marketing Date 20100525
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name BUPRENORPHINE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA]

Complete Information of Buprenorphine Hydrochloride


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