NDCFind

Buprenorphine 00228-3153-03

Package NDC

00228-3153-03

Product NDC: 00228-3153

Manufacturer
Actavis Pharma, Inc.
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
February 19, 2015
Listing Expires
December 31, 2027
Application
ANDA090819

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

Partial Opioid Agonist [EPC]Partial Opioid Agonists [MoA]

Selected Package

00228-3153-03Selected

30 TABLET in 1 BOTTLE (0228-3153-03)