NDCFind

Buprenorphine 60687-0492-21

Package NDC

60687-0492-21

Product NDC: 60687-0492

Manufacturer
American Health Packaging
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
February 6, 2020
Listing Expires
December 31, 2026
Application
ANDA207276

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

60687-0492-21Selected

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-492-21) / 1 TABLET in 1 BLISTER PACK (60687-492-11)