NDC 71335-1858

BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE 2 mg / 8 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Accord Healthcare Inc.'s NDC 16729-550.

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 / 8 mg
Approval
ANDA ANDA209069
On the market since
Jan 22, 2021
Package NDCs
71335-1858-0 71335-1858-1 71335-1858-2 71335-1858-3 71335-1858-4 71335-1858-5 71335-1858-6 71335-1858-7 71335-1858-8 71335-1858-9
Official label
DailyMed (National Library of Medicine), updated Nov 16, 2023

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