NDC 51862-610
Methylphenidate Hydrochloride (LA) 20 mg capsule, extended release
On the label: Mayne Pharma Inc..
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that packages it and labels it). 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 Mayne Pharma Inc. names for other drugs.
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- capsule, extended release
- Strength
- 20 mg
- Approval
- ANDA ANDA078458
- On the market since
- Dec 6, 2018
- Package NDCs
51862-610-01- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2025
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