Oxycodone Hydrochloride

Product NDC

62559-152

11-digit product format

625590152

Labeler code

62559

Product ID

62559-152_23a53880-bc47-4102-82ea-4ec6dfe32709

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone Hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

ANI Pharmaceuticals, Inc.

Application

ANDA203447

Marketing category

ANDA

Marketing start

2017-09-01

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE

Active strength

100 mg/5mL

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