NDC 70518-4571
buprenorphine hydrochloride 8 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-2038.
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 Pharmaceutical Associates, Inc. names for other drugs.
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 8 mg
- Approval
- ANDA ANDA090622
- On the market since
- Feb 10, 2026
- Package NDCs
70518-4571-070518-4571-170518-4571-2- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
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