NDCFind

Buprenorphine Sublingual 72189-0579-60

Package NDC

72189-0579-60

Product NDC: 72189-0579

Manufacturer
Direct_rx
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
September 13, 2024
Listing Expires
December 31, 2026
Application
ANDA201760

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride2 mg/1

Drug Class

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

Selected Package

72189-0579-60Selected

60 TABLET in 1 BOTTLE (72189-579-60)