NDC 0115-9921-01
Dexmethylphenidate hydrochloride 20 mg/1
Dexmethylphenidate hydrochloride · CAPSULE, EXTENDED RELEASE
Dexmethylphenidate hydrochloride is a prescription stimulant medication used to treat attention-deficit/hyperactivity disorder (ADHD) in children and adults. This extended-release capsule formulation is designed to provide symptom relief throughout the day.
Key Facts
- Brand Name
- Dexmethylphenidate hydrochloride
- Generic Name
- Dexmethylphenidate hydrochloride
- NDC Code (Package)
0115-9921-01- NDC Code (Product)
0115-9921- Manufacturer
- Amneal Pharmaceuticals of New York LLC
- Strength
- 20 mg/1
- Dosage Form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule II (Controlled)
- Application #
- ANDA079108
- Marketing Start
- 12/21/2015
Recall History
No Recall HistoryView Full Drug Page
Dexmethylphenidate hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.