NDCFind

Buprenorphine Hcl 31722-0871-30

Package NDC

31722-0871-30

Product NDC: 31722-0871

Manufacturer
Camber Pharmaceuticals, Inc.
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
January 12, 2026
Listing Expires
December 31, 2027
Application
ANDA219401

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

31722-0871-30Selected

30 TABLET in 1 BOTTLE (31722-871-30)