NDC 57664-230
Methylphenidate Hydrochloride 20 mg tablet
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ohm Laboratories Inc. | New Brunswick, NJ, United States | Makes it | No problems foundOct 31, 2024 · 22 inspections |
Recalls
- Jul 13, 2023 · Class II · Sun Pharmaceutical Industries Inc
Presence of Foreign Substance: Metal embedded in a tablet.
Lots: Lot AC74459, Exp 07/31/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA090710
- On the market since
- Aug 16, 2013
- Package NDCs
57664-230-0857664-230-1357664-230-1857664-230-8357664-230-88- Official label
- DailyMed (National Library of Medicine), updated Feb 27, 2025
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