NDC 10135-741

Bisoprolol Fumarate and Hydrochlorothiazide 5 mg / 6.25 mg tablet

On the label: Marlex Pharmaceuticals, Inc.. It's repackaged: Marlex Pharmaceuticals, Inc. rebottles it from ANI Pharmaceuticals, Inc.'s NDC 70954-413.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Novitium Pharma LLCEast Windsor, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 16, 2024 · 5 inspections

Product details

Generic drug
Bisoprolol and Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
5 mg / 6.25 mg
Approval
ANDA ANDA215562
On the market since
May 1, 2022
Package NDCs
10135-741-01 10135-741-05
Official label
DailyMed (National Library of Medicine), updated Sep 23, 2025

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