Oxycodone Hydrochloride

Product NDC

63629-4184

11-digit product format

636294184

Labeler code

63629

Product ID

63629-4184_dbc5254f-4f73-49ee-a8af-b3280963a05a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077712

Marketing category

ANDA

Marketing start

2009-03-02

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE

Active strength

5 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