Oxycodone Hydrochloride

Product NDC

63629-3803

11-digit product format

636293803

Labeler code

63629

Product ID

63629-3803_e4355d25-edd6-4289-b54e-c3b222f13a1a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

NDA200534

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-12-15

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record