Methylphenidate Hydrochloride (LA)

Product NDC

51862-263

11-digit product format

518620263

Labeler code

51862

Product ID

51862-263_85816e52-e2b6-4757-bf64-bfcd52079b19

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methylphenidate Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Mayne Pharma

Application

ANDA078458

Marketing category

ANDA

Marketing start

2016-08-03

Marketing end

2020-01-31

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

0000-00-00

Current FDA listing

Historical FDA.report record