NDC 87063-198
Ropinirole 0.25 mg tablet, film coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Bionpharma Inc.'s NDC 69452-356.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Optimus Pharma Private Limited | Hyderabad, India | Makes it, tests it and labels it | Problems found, fixed voluntarilyOct 1, 2025 · 3 inspections |
| OrBion Pharmaceuticals Private Limited | Kancheepuram, India | Makes it, tests it, packages it and labels it | No problems foundOct 27, 2025 · 6 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ropinirole: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 0.25 mg
- Approval
- ANDA ANDA079229
- On the market since
- Sep 15, 2022
- Package NDCs
87063-198-0187063-198-3087063-198-6087063-198-90- Official label
- DailyMed (National Library of Medicine), updated May 7, 2026
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