NDC 0406-8005
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate 2 mg / 0.5 mg tablet
On the label: SpecGx LLC.
Where it's 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.
Product details
- Generic drug
- Buprenorphine and Naloxone: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg / 0.5 mg
- Approval
- ANDA ANDA207000
- On the market since
- Dec 13, 2017
- Package NDCs
0406-8005-03- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
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