NDC 43386-861
Dexmethylphenidate Hydrochloride 10 mg tablet
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novel Laboratories, Inc. | Somerset, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Dexmethylphenidate: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA204534
- On the market since
- Dec 4, 2015
- Package NDCs
43386-861-0143386-861-0343386-861-10- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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