OXYCODONE HYDROCHLORIDE

Product NDC

61919-821

11-digit product format

619190821

Labeler code

61919

Product ID

61919-821_8d2c450a-a72f-39ed-e053-2995a90abd5f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

OXYCODONE HYDROCHLORIDE

Dosage form

TABLET

Route

ORAL

Labeler

Direct_Rx

Application

ANDA203638

Marketing category

ANDA

Marketing start

2019-07-08

Marketing end

0000-00-00

Substance

OXYCODONE HYDROCHLORIDE

Active strength

5 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