NDC 0781-2361 – Methylphenidate

Methylphenidate Hydrochloride 10 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0781-2361

Product details

Brand name
Methylphenidate
Generic name
Methylphenidate
Labeler
Sandoz Inc
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021284
Marketed since
November 24, 2015
Marketing end
April 30, 2027
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Methylphenidate →

Package NDC codes (1)

Package NDCDescriptionSince
0781-2361-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2361-01)Feb 28, 2018

Other Methylphenidate products