NDC 67877-655
Dexmethylphenidate Hydrochloride 2.5 mg tablet
On the label: Ascend Laboratories, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it | No problems foundAug 30, 2019 · 6 inspections |
Product details
- Generic drug
- Dexmethylphenidate: every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA212631
- On the market since
- Jul 21, 2019
- Package NDCs
67877-655-0167877-655-0567877-655-30- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2024
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