METOPROLOL SUCCINATE

Product NDC

49884-406

11-digit product format

498840406

Labeler code

49884

Product ID

49884-406_fcca559c-280e-4e44-b70c-6fe89ee3a277

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol succinate

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Par Pharmaceutical Inc.

Application

NDA019962

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2007-07-26

Marketing end

2019-09-30

Substance

METOPROLOL SUCCINATE

Active strength

100 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