Methylphenidate Hydrochloride (LA)

Product NDC

0093-3230

11-digit product format

000933230

Labeler code

0093

Product ID

0093-3230_c5fe9cb8-7e45-4644-a5e3-0cfa0c3c1951

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methylphenidate Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA078458

Marketing category

ANDA

Marketing start

2018-01-02

Marketing end

2020-07-31

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