NDC 68084-823
Methylphenidate Hydrochloride 10 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from SpecGx LLC's NDC 0406-1144.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| SpecGx LLC | Hobart, NY, United States | Makes it and tests it | No problems foundMar 13, 2020 · 6 inspections |
| SpecGx LLC | St. Louis, MO, United States | Makes the active ingredient | Problems found, fixed voluntarilyOct 22, 2025 · 8 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA040300
- On the market since
- Sep 30, 2014
- Package NDCs
68084-823-1168084-823-21- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2025
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