NDC 51407-948
buprenorphine hydrochloride and naloxone hydrochloride dihydrate 2 mg / 0.5 mg tablet
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0188.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Repackaging site
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
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
51407-948-30- Official label
- DailyMed (National Library of Medicine), updated Sep 21, 2026
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