NDC 58118-3268
Venlafaxine Hydrochloride 225 mg tablet, extended release
On the label: Clinical Solutions Wholesale. It's repackaged from NDC 0131-3268, made by UCB, Inc. (venlafaxine 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 and relabels 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 Clinical Solutions Wholesale names for other drugs.
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release
- Strength
- 225 mg
- Approval
- NDA NDA022104
- On the market since
- Apr 29, 2010
- Package NDCs
58118-3268-058118-3268-358118-3268-858118-3268-9- Official label
- DailyMed (National Library of Medicine), updated Aug 13, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?