NDC 13811-708
Methylphenidate Hydrochloride 36 mg tablet, extended release
On the label: Trigen Laboratories, LLC.
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 Trigen Laboratories, LLC names for other drugs.
Recalls
- Jun 17, 2024 · Class II · Trigen Laboratories
Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.
Lots: Lot 230159M, Exp Date 2/28/2026 - Feb 28, 2018 · Class III · Osmotica Pharmaceutical Corp
Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER Tablets 36 mg found to contain 1 27 mg Methylphenidate HCL ER Tablet.
Lots: Lots: 170231B, 170232A, 170233A, 170234A - Dec 18, 2017 · Class III · Osmotica Pharmaceutical Corp
Subpotent Drug
Lots: Lot #: 170027A, Exp. 02/2019 - Dec 18, 2017 · Class III · Osmotica Pharmaceutical Corp
Subpotent Drug
Lots: Lot #: 170029A, Exp. 02/2019; 170030A, Exp. 02/2019
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, extended release, oral
- Strength
- 36 mg
- Approval
- ANDA ANDA205327
- On the market since
- Aug 14, 2017
- Package NDCs
13811-708-10- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2026
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