Dexmethylphenidate Hydrochloride

Product NDC

0093-5275

11-digit product format

000935275

Labeler code

0093

Product ID

0093-5275_f9638001-2499-4448-a49b-948b263ee562

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dexmethylphenidate Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA077107

Marketing category

ANDA

Marketing start

2007-06-08

Marketing end

2020-05-31

Substance

DEXMETHYLPHENIDATE HYDROCHLORIDE

Active strength

3 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