Store at 25ºC (77ºF); excursions permitted to 15-30ºC (59-86ºF) [see USP Controlled Room Temperature]. Protect from moisture.

Dispense in tight, light-resistant container (USP).

To report SUSPECTED ADVERSE REACTIONS, contact Novartis Pharmaceuticals Corporation at 1 - 888 - 669 - 6682 or FDA at 1 - 800 - FDA - 1088 or www.fda.gov/medwatch

Manufactured by:

Novartis Pharmaceuticals Corporation

Suffern, New York 10901

Distributed by:

Novartis Pharmaceuticals Corporation

East Hanover, New Jersey 07936

REV: MARCH 2009     T2009-42

Package Label – 50/25

Rx Only          NDC 0078-0460-05

Lopressor HCT®

metoprolol tartrate USP 50 mg

hydrochlorothiazide USP 25 mg

100 Tablets

Dispense in tight, light-resistant container (USP).

Package Label – 100/25

Rx Only          NDC 0078-0461-05

Lopressor HCT®

metoprolol tartrate USP 100 mg

hydrochlorothiazide USP 25 mg

100 Tablets

Dispense in tight, light-resistant container (USP).

Package Label – 100/50

Rx Only          NDC 0078-0462-05

Lopressor HCT®

metoprolol tartrate USP 100 mg

hydrochlorothiazide USP 50 mg

100 Tablets

Dispense in tight, light-resistant container (USP).

Manufacturer

Novartis Pharmaceuticals Corporation (NPC), a US subsidiary of Novartis AG

Active Ingredients

Source

• U.S. National Library of Medicine
• DailyMed
•  Last Updated: 2nd of March 2011