OXYCODONE HCl

Product NDC

63304-683

11-digit product format

633040683

Labeler code

63304

Product ID

63304-683_056f088d-cff1-4b46-8539-ff85880586bf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Ranbaxy Pharmaceuticals Inc.

Application

NDA022272

Marketing category

NDA

Marketing start

2010-08-08

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE

Active strength

40 mg/1

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record