Metoprolol Tartrate

Product NDC

51079-802

11-digit product format

510790802

Labeler code

51079

Product ID

51079-802_9c31e564-de0c-7d34-e053-2995a90a2db9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

metoprolol tartrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076704

Marketing category

ANDA

Marketing start

1994-05-03

Marketing end

2020-06-30

Substance

METOPROLOL TARTRATE

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