methylphenidate hydrochloride

Product NDC

68084-829

11-digit product format

680840829

Labeler code

68084

Product ID

68084-829_951f9025-3dc9-8e0b-e053-2a95a90ac51a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methylphenidate hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

NDA021121

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-08-21

Marketing end

2020-09-30

Substance

METHYLPHENIDATE HYDROCHLORIDE

Active strength

36 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