Drugplain

NDC 0115-1740-01

Methylphenidate Hydrochloride 50 mg/1

Methylphenidate Hydrochloride · CAPSULE, EXTENDED RELEASE

No Recall History

Methylphenidate Hydrochloride is a capsule, extended release containing methylphenidate hydrochloride at a strength of 50 mg/1. Manufactured by Amneal Pharmaceuticals of New York LLC.

Key Facts

Brand Name
Methylphenidate Hydrochloride
Generic Name
Methylphenidate Hydrochloride
NDC Code (Package)
0115-1740-01
NDC Code (Product)
0115-1740
Manufacturer
Amneal Pharmaceuticals of New York LLC
Strength
50 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
DEA Schedule
Schedule II (Controlled)
Application #
ANDA205105
Marketing Start
09/20/2016

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.