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 Sandoz Inc. names for other drugs.
Recalls
- Jun 1, 2026 · Class III · Sandoz Inc
Labeling: Incorrect or Missing Lot and/or Exp Date
Lots: Lot VA0099422; Exp. Date June 30, 2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dexmethylphenidate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 15 mg
- Approval
- NDA NDA021802
- On the market since
- May 31, 2005
- Package NDCs
66758-237-0166758-237-31- Official label
- DailyMed (National Library of Medicine), updated Sep 23, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?