NDC 0527-8112
Dexmethylphenidate HydrochlorideExtended-Release 35 mg capsule, extended release
On the label: Lannett Company, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lannett Company, Inc. names for other drugs.
Product details
- Generic drug
- Dexmethylphenidate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 35 mg
- Approval
- ANDA ANDA210279
- On the market since
- Oct 9, 2018
- Package NDCs
0527-8112-37- Official label
- DailyMed (National Library of Medicine), updated Sep 25, 2025
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