NDC 67877-615
Methylphenidate hydrochloride 20 mg tablet, extended release
On the label: Ascend Laboratories, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories | Location not on file | Makes it, tests it and packages it | Not inspected on record |
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, extended release
- Strength
- 20 mg
- Approval
- ANDA ANDA212288
- On the market since
- Oct 8, 2020
- Package NDCs
67877-615-01- Official label
- DailyMed (National Library of Medicine), updated Sep 20, 2022
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