NDC 55648-771
Ropinirole Hydrochloride 2 mg tablet, film coated, 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
- Ropinirole: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 2 mg
- Approval
- ANDA ANDA091395
- On the market since
- Aug 15, 2012
- Package NDCs
55648-771-0155648-771-0255648-771-0355648-771-0455648-771-05- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2012
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