NDC 13811-708-10
Methylphenidate Hydrochloride 36 mg/1
Methylphenidate hydrochloride · TABLET, EXTENDED RELEASE
Methylphenidate Hydrochloride is a tablet, extended release containing methylphenidate hydrochloride at a strength of 36 mg/1. Manufactured by Trigen Laboratories, LLC.
Key Facts
- Brand Name
- Methylphenidate Hydrochloride
- Generic Name
- Methylphenidate hydrochloride
- NDC Code (Package)
13811-708-10- NDC Code (Product)
13811-708- Manufacturer
- Trigen Laboratories, LLC
- Strength
- 36 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA205327
- Marketing Start
- 08/14/2017
Recall History
No Recall HistoryView Full Drug Page
Methylphenidate Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.