Methylphenidate Hydrochloride

Product NDC

64720-402

11-digit product format

647200402

Labeler code

64720

Product ID

64720-402_72cf9b08-1cc5-423e-b51e-95e57e6665c0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methylphenidate Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

CorePharma, LLC

Application

ANDA205105

Marketing category

ANDA

Marketing start

2016-09-20

Marketing end

2019-10-01

Substance

METHYLPHENIDATE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record