OxyContin

Product NDC

42254-159

11-digit product format

422540159

Labeler code

42254

Product ID

42254-159_d1f543fe-ebfb-4ace-a223-d928d6b648c1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Rebel Distributors Corp

Application

NDA022272

Marketing category

NDA

Marketing start

2010-08-08

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA],Opioid Agonist [EPC]

DEA schedule

CII

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record