NDCFind

Buprenorphine And Naloxone 60687-0637-65

Package NDC

60687-0637-65

Product NDC: 60687-0637

Manufacturer
American Health Packaging
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
March 14, 2022
Listing Expires
December 31, 2026
Application
ANDA205601

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1
Naloxone Hydrochloride Dihydrate2 mg/1

Drug Class

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

Selected Package

60687-0637-65Selected

50 BLISTER PACK in 1 CARTON (60687-637-65) / 1 TABLET in 1 BLISTER PACK (60687-637-11)