NDC 67046-990
buprenorphine hydrochloride 2 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 50383-924, made by Akorn Operating Company LLC (dba Akorn) (buprenorphine hydrochloride). 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
- 2 mg
- Approval
- ANDA ANDA090622
- On the market since
- Sep 24, 2010
- Package NDCs
67046-990-30- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2017
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