Oxycodone and Acetaminophen

Product NDC

70700-105

11-digit product format

707000105

Labeler code

70700

Product ID

70700-105_520ada9f-f0c6-9ba5-162a-025dcd62623f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone and Acetaminophen

Dosage form

TABLET

Route

ORAL

Labeler

Xiromed, LLC

Application

ANDA207574

Marketing category

ANDA

Marketing start

2018-08-29

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

2020-12-31

Current FDA listing

Historical FDA.report record