NDC 68151-3659
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Carilion Materials Management. It's repackaged from NDC 59762-0180, made by Greenstone LLC (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). 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 Carilion Materials Management names for other drugs.
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release
- Strength
- 37.5 mg
- Approval
- NDA AUTHORIZED GENERIC NDA020699
- On the market since
- Jun 2, 2011
- Package NDCs
68151-3659-7- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2015
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