NDC 65162-231
Methylphenidate Hydrochloride 18 mg tablet, extended release
On the label: Amneal Pharmaceuticals.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals of New York, LLC | Brookhaven, NY, United States | Makes it, tests it, packages it and labels it | No problems foundSep 25, 2026 · 14 inspections |
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, extended release
- Strength
- 18 mg
- Approval
- ANDA ANDA207515
- On the market since
- Feb 2, 2018
- Package NDCs
65162-231-0365162-231-09- Official label
- DailyMed (National Library of Medicine), updated May 15, 2024
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