oxycodone hydrochloride

Product NDC

0781-5767

11-digit product format

007815767

Labeler code

0781

Product ID

0781-5767_2daac07a-7b11-4e90-bc56-20a4f54fbbf8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Sandoz Inc

Application

NDA022272

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-10-08

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record