oxycodone and acetaminophen

Product NDC

71335-0221

11-digit product format

713350221

Labeler code

71335

Product ID

71335-0221_ef7e851d-c5ad-45e3-a562-de692b83ddbe

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxycodone and acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA090535

Marketing category

ANDA

Marketing start

2015-11-02

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