NDC 0185-0325

Benazepril Hydrochloride and Hydrochlorothiazide 10 mg / 12.5 mg tablet, film coated

On the label: Sandoz Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sandoz Inc. names for other drugs.

Product details

Generic drug
Benazeprilat and Hydrochlorothiazide: every company that makes it
Form
tablet, film coated, oral
Strength
10 mg / 12.5 mg
Approval
ANDA ANDA076631
On the market since
Apr 4, 2014
Package NDCs
0185-0325-01
Official label
DailyMed (National Library of Medicine), updated Jun 14, 2025

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