Metoprolol Succinate

Product NDC

62037-830

11-digit product format

620370830

Labeler code

62037

Product ID

62037-830_2db39c73-6577-49b0-961c-63b30a61b181

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol Succinate

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA076862

Marketing category

ANDA

Marketing start

2009-08-04

Marketing end

2020-09-30

Substance

METOPROLOL SUCCINATE

Active strength

25 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