NDC 62037-725
Methylphenidate Hydrochloride 18 mg tablet, film coated, extended release
On the label: Actavis Pharma, 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 Actavis Pharma, Inc. names for other drugs.
Recalls
- Jan 27, 2020 · Class II · Teva Pharmaceuticals USA
CGMP deviations: Product bottle may be absent of desiccant.
Lots: Lot #: 1332796 A, Exp 11/2020 - Jan 27, 2020 · Class II · Teva Pharmaceuticals USA
CGMP deviations: Product bottle may be absent of desiccant.
Lots: Lot # 1332799A, Exp 11/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 18 mg
- Approval
- ANDA ANDA076772
- On the market since
- Mar 4, 2019
- Package NDCs
62037-725-01- Official label
- DailyMed (National Library of Medicine), updated Apr 30, 2026
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