NDC 70010-010
Dexmethylphenidate Hydrochloride 35 mg capsule, extended release
On the label: Granules Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granules Pharmaceuticals Inc. | Chantilly, VA, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 3, 2026 · 6 inspections |
Product details
- Generic drug
- Dexmethylphenidate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 35 mg
- Approval
- ANDA ANDA213813
- On the market since
- Dec 1, 2020
- Package NDCs
70010-010-01- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2026
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