NDC 0121-1019
buprenorphine hydrochloride 2 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: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg
- Approval
- ANDA ANDA090622
- On the market since
- Oct 12, 2023
- Package NDCs
0121-1019-30- Official label
- DailyMed (National Library of Medicine), updated Feb 28, 2026
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