NDC 70518-1557
Buprenorphine 2 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Actavis Pharma, Inc.'s NDC 0228-3156.
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 Actavis Pharma, Inc. names for other drugs.
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2 mg
- Approval
- ANDA ANDA090819
- On the market since
- Oct 19, 2018
- Package NDCs
70518-1557-070518-1557-170518-1557-2- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
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