NDCFind

Buprenorphine 50268-0129-15

Package NDC

50268-0129-15

Product NDC: 50268-0129

Manufacturer
Avpak
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
March 19, 2024
Listing Expires
December 31, 2027
Application
ANDA201760

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

50268-0129-15Selected

50 BLISTER PACK in 1 BOX (50268-129-15) / 1 TABLET in 1 BLISTER PACK (50268-129-11)