Metoprolol Succinate

Product NDC

62037-833

11-digit product format

620370833

Labeler code

62037

Product ID

62037-833_d1d2d8db-a424-49c2-8721-3f1b36b07067

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol Succinate

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA077298

Marketing category

ANDA

Marketing start

2010-04-15

Marketing end

2021-01-31

Substance

METOPROLOL SUCCINATE

Active strength

200 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record