Metoprolol Tartrate

Product NDC

50436-3155

11-digit product format

504363155

Labeler code

50436

Product ID

50436-3155_a8d7b233-9e82-4be0-815e-52ecd61abc32

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol Tartrate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA078459

Marketing category

ANDA

Marketing start

2009-03-24

Marketing end

0000-00-00

Substance

METOPROLOL TARTRATE

Active strength

25 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record