METHADOSE DISPERSIBLE

Product NDC

60687-209

11-digit product format

606870209

Labeler code

60687

Product ID

60687-209_7351d4d4-6024-7a84-e053-2a91aa0aa8bf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methadone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA074184

Marketing category

ANDA

Marketing start

2016-07-19

Marketing end

2019-11-30

Substance

METHADONE HYDROCHLORIDE

Active strength

40 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