NDC 0185-0236
Benazepril Hydrochloride and Hydrochlorothiazide 5 mg / 6.25 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
- 5 mg / 6.25 mg
- Approval
- ANDA ANDA076631
- On the market since
- Mar 17, 2015
- Package NDCs
0185-0236-01- Official label
- DailyMed (National Library of Medicine), updated Jun 14, 2025
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