NDC 0121-1018
Buprenorphine and Naloxone 2 mg / 0.5 mg tablet
On the label: Pharmaceutical Associates, Inc..
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 Pharmaceutical Associates, Inc. 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 ANDA204431
- On the market since
- Sep 5, 2023
- Package NDCs
0121-1018-30- Official label
- DailyMed (National Library of Medicine), updated Feb 28, 2026
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