Dexmethylphenidate Hydrochloride

Product NDC

0527-1900

11-digit product format

005271900

Labeler code

0527

Product ID

0527-1900_0c69f111-f3c3-4ecb-a8ae-05c5531632db

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dexmethylphenidate Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Lannett Company, Inc.

Application

ANDA209468

Marketing category

ANDA

Marketing start

2017-09-25

Marketing end

0000-00-00

Substance

DEXMETHYLPHENIDATE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record