oxycodone hydrochloride

Product NDC

49884-138

11-digit product format

498840138

Labeler code

49884

Product ID

49884-138_1a82d9cc-a636-4838-a50f-ed542fa5cd26

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

NDA022272

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-08-08

Marketing end

2020-12-31

Substance

OXYCODONE HYDROCHLORIDE

Active strength

40 mg/1

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record