NDC 72888-182

buprenorphine hydrochloride 2 mg tablet

On the label: Advagen Pharma Ltd..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Rubicon Research LimitedThane, IndiaMakes it, tests it, packages it and labels it No problems foundMar 8, 2024 · 5 inspections

Product details

Generic drug
Buprenorphine: every company that makes it
Form
tablet, sublingual
Strength
2 mg
Approval
ANDA ANDA090279
On the market since
Jun 10, 2015
Package NDCs
72888-182-30 72888-182-90
Official label
DailyMed (National Library of Medicine), updated Jul 17, 2026

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