Methadone Hydrochloride

Product NDC

63739-006

11-digit product format

637390006

Labeler code

63739

Product ID

63739-006_851d8b07-d57f-4c94-8406-542506b0c0d7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methadone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA090635

Marketing category

ANDA

Marketing start

2012-01-16

Marketing end

0000-00-00

Substance

METHADONE HYDROCHLORIDE

Active strength

10 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