NDC 57664-710
Methylphenidate Hydrochloride 72 mg tablet, extended release
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, tests it and packages it | No problems foundOct 31, 2024 · 22 inspections |
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 72 mg
- Approval
- ANDA ANDA217229
- On the market since
- Dec 20, 2024
- Package NDCs
57664-710-8357664-710-88- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2026
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