Oxycodone Hydrochloride

Product NDC

0603-4994

11-digit product format

006034994

Labeler code

0603

Product ID

0603-4994_54873134-c3ba-43c2-98b1-df36c08c74d0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA077712

Marketing category

ANDA

Marketing start

2015-04-13

Marketing end

2020-02-29

Substance

OXYCODONE HYDROCHLORIDE

Active strength

20 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