NDC 68462-579
Benazepril Hydrochloride and Hydrochlorothiazide 20 mg / 25 mg tablet, film coated
On the label: Glenmark Pharmaceuticals Inc., USA.
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 Glenmark Pharmaceuticals Inc., USA names for other drugs.
Product details
- Generic drug
- Benazeprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 25 mg
- Approval
- ANDA ANDA076631
- On the market since
- Feb 11, 2004
- Package NDCs
68462-579-01- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2023
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