NDCFind

Buprenorphine 00904-7154-04

Package NDC

00904-7154-04

Product NDC: 00904-7154

Manufacturer
Major Pharmaceuticals
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
October 8, 2009
Listing Expires
December 31, 2027
Application
ANDA078633

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride2 mg/1

Drug Class

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

Selected Package

00904-7154-04Selected

30 BLISTER PACK in 1 CARTON (0904-7154-04) / 1 TABLET in 1 BLISTER PACK