NDC 67046-997
Buprenorphine Hydrochloride Sublingual 8 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 0378-0924, made by Mylan Pharmaceuticals Inc. (Buprenorphine Hydrochloride Sublingual). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Coupler Enterprises Inc. names for other drugs.
Product details
- Generic drug
- Buprenorphine: every company that makes it
- Form
- tablet
- Strength
- 8 mg
- Approval
- ANDA ANDA201066
- On the market since
- Mar 6, 2015
- Package NDCs
67046-997-30- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2017
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