NDC 58118-0549

BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE 2 mg / 0.5 mg tablet

On the label: Clinical Solutions Wholesale. It's repackaged: Clinical Solutions Wholesale rebottles it from Accord Healthcare Inc.'s NDC 16729-549.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Wes Pharma IncWestminster, MD, United StatesMakes it Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections

Repackaging site

Product details

Generic drug
Buprenorphine and Naloxone: every company that makes it
Form
tablet, sublingual
Strength
2 mg / 0.5 mg
Approval
ANDA ANDA209069
On the market since
Sep 1, 2020
Package NDCs
58118-0549-8
Official label
DailyMed (National Library of Medicine), updated Mar 5, 2026

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