NDC 55648-716
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Wockhardt Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Wockhardt Limited | Location not on file | Makes it, tests it, packages it and labels it | Not inspected on record |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release
- Strength
- 37.5 mg
- Approval
- ANDA ANDA078865
- On the market since
- Apr 14, 2011
- Package NDCs
55648-716-0155648-716-0255648-716-0355648-716-0455648-716-05- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2014
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