methylphenidate hydrochloride CD

Product NDC

62175-154

11-digit product format

621750154

Labeler code

62175

Product ID

62175-154_86c43193-60a3-454c-94ed-6e1fcbd1b835

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methylphenidate hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Kremers Urban Pharmaceuticals Inc.

Application

NDA021259

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2006-03-21

Marketing end

2020-07-31

Substance

METHYLPHENIDATE HYDROCHLORIDE

Active strength

40 mg/1

Pharmacologic classes

Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record