Oxycodone Hydrochloride

Product NDC

68084-828

11-digit product format

680840828

Labeler code

68084

Product ID

68084-828_8176bebf-bb0d-7c11-e053-2a91aa0a08be

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxycodone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077290

Marketing category

ANDA

Marketing start

2014-09-18

Marketing end

2019-08-31

Substance

OXYCODONE HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA],Opioid Agonist [EPC]

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record