NDC 31722-851

Buprenorphine and Naloxone 2 mg / 8 mg tablet

On the label: Camber Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Buprenorphine and Naloxone: every company that makes it
Form
tablet, sublingual
Strength
2 mg / 8 mg
Approval
ANDA ANDA219727
On the market since
Jan 5, 2026
Package NDCs
31722-851-30
Official label
DailyMed (National Library of Medicine), updated Jan 28, 2026

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