Oxycodone and Acetaminophen

Product NDC

42291-646

11-digit product format

422910646

Labeler code

42291

Product ID

42291-646_834a7ea8-a251-6797-e053-2a91aa0a260c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone and Acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA040778

Marketing category

ANDA

Marketing start

2016-02-18

Marketing end

2019-03-31

Substance

OXYCODONE HYDRO

Active strength

10 mg/1; mg/1

Pharmacologic classes

Full Opioid Ago

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record