Oxymorphone Hydrochloride

Product NDC

60951-795

11-digit product format

609510795

Labeler code

60951

Product ID

60951-795_a35dcd4f-ccff-4d86-87e3-5775a869dfaf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxymorphone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical

Application

NDA021611

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-09-29

Marketing end

2020-07-31

Substance

OXYMORPHONE HYDROCHLORIDE

Active strength

10 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