NDC 87441-002
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate 2 mg / 8 mg tablet
On the label: Unit Dose Solutions, Inc.. It's repackaged: Unit Dose Solutions, Inc. rebottles it from SpecGx LLC's NDC 0406-8020.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants SpecGx LLC names for other drugs.
Repackaging site
- Unit Dose Solutions, Inc., Raleigh, NC, United States · repackages it
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg / 8 mg
- Approval
- ANDA ANDA207000
- On the market since
- Apr 13, 2026
- Package NDCs
87441-002-01- Official label
- DailyMed (National Library of Medicine), updated Apr 16, 2026
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