PERCOCET

Product NDC

65084-298

11-digit product format

650840298

Labeler code

65084

Product ID

65084-298_81152a6d-7c01-432e-a811-f3ffb00435fa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone hydrochloride and acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

Mckesson Rxpak Inc

Application

ANDA040330

Marketing category

ANDA

Marketing start

1999-06-30

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN

Active strength

5 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