NDC 10702-076
Methylphenidate Hydrochloride Extended Release 20 mg tablet
On the label: KVK-TECH, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA207488
- On the market since
- Jun 9, 2015
- Package NDCs
10702-076-0110702-076-06- Official label
- DailyMed (National Library of Medicine), updated Oct 7, 2025
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