NDC 71335-1653

buprenorphine hydrochloride and naloxone hydrochloride dihydrate 2 mg / 0.5 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0188.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
West-Ward Columbus Inc.Columbus, OH, United StatesMakes it No problems foundApr 30, 2026 · 27 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 ANDA203326
On the market since
Jun 27, 2014
Package NDCs
71335-1653-1
Official label
DailyMed (National Library of Medicine), updated May 13, 2026

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