Methadone hydrochloride

Product NDC

57664-602

11-digit product format

576640602

Labeler code

57664

Product ID

57664-602_9ec58c52-1baf-4d56-aed2-6a853151ed92

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methadone hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Sun Pharmaceutical Industries, Inc.

Application

ANDA208305

Marketing category

ANDA

Marketing start

2018-04-17

Marketing end

0000-00-00

Substance

METHADONE HYDROCHLORIDE

Active strength

5 mg/1001

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