oxycodone and acetaminophen

Product NDC

46672-196

11-digit product format

466720196

Labeler code

46672

Product ID

46672-196_abc1dd98-7e59-6815-e053-2995a90a01db

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone and acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

Mikart, LLC

Application

ANDA040608

Marketing category

ANDA

Marketing start

2005-12-30

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

2021-12-31

Current FDA listing

Historical FDA.report record