OxyContin

Product NDC

21695-941

11-digit product format

216950941

Labeler code

21695

Product ID

21695-941_8c9cb953-0995-4f47-83ee-c8c9dfd1b533

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

80 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