OXYCODONE HYDROCHLORIDE

Product NDC

63739-365

11-digit product format

637390365

Labeler code

63739

Product ID

63739-365_8207a902-7f93-4f49-a576-d2123405f25c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

OXYCODONE HYDROCHLORIDE

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA077290

Marketing category

ANDA

Marketing start

2012-12-26

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA],Opioid Agonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record