Oxycodone and Acetaminophen

Product NDC

63739-739

11-digit product format

637390739

Labeler code

63739

Product ID

63739-739_306cf024-d7ef-4fff-ab49-a4e6c4bc9af3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone and Acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA202677

Marketing category

ANDA

Marketing start

2012-01-17

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN

Active strength

10 mg/1; 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