Dexmethylphenidate hydrochloride

Product NDC

63629-1096

11-digit product format

636291096

Labeler code

63629

Product ID

63629-1096_b4053bd8-6d5b-4d57-b0a8-8a901a3cebe2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Dexmethylphenidate hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA201231

Marketing category

ANDA

Marketing start

2020-06-17

Marketing end

0000-00-00

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

2021-12-31

Current FDA listing

Historical FDA.report record