methylphenidate hydrochloride CD

Product NDC

62175-153

11-digit product format

621750153

Labeler code

62175

Product ID

62175-153_61b09a60-9f35-41ae-8b90-620589ef32f9

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

2003-07-22

Marketing end

0000-00-00

Substance

METHYLPHENIDATE HYDROCHLORIDE

Active strength

30 mg/1

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record