Methylphenidate Hydrochloride

Product NDC

63629-1083

11-digit product format

636291083

Labeler code

63629

Product ID

63629-1083_cd1d2e26-dc7d-4627-9c89-261ea560082b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methylphenidate Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA090710

Marketing category

ANDA

Marketing start

2020-06-17

Marketing end

0000-00-00

Substance

METHYLPHENIDATE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record