Metoprolol Tartrate and Hydrochlorothiazide

Product NDC

13811-670

11-digit product format

138110670

Labeler code

13811

Product ID

13811-670_18fe1a05-215b-445b-b309-580660325a43

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoprolol Tartrate and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Trigen Laboratories, LLC

Application

ANDA202870

Marketing category

ANDA

Marketing start

2013-09-17

Marketing end

0000-00-00

Substance

METOPROLOL TARTRATE; HYDROCHLOROTHIAZIDE

Active strength

100 mg/1; mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record