NDCFind

Buprenorphine And Naloxone 31722-0850-30

Package NDC

31722-0850-30

Product NDC: 31722-0850

Manufacturer
Camber Pharmaceuticals, Inc.
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
January 5, 2026
Listing Expires
December 31, 2027
Application
ANDA219727

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride2 mg/1
Naloxone Hydrochloride Dihydrate.5 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]Partial Opioid Agonist [EPC]

Selected Package

31722-0850-30Selected

30 TABLET in 1 BOTTLE (31722-850-30)