NDC 0574-0229
benazepril hydrochloride and hydrochlorothiazide 20 mg / 12.5 mg tablet
On the label: Padagis US LLC.
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 Padagis US LLC names for other drugs.
Product details
- Generic drug
- Benazeprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg / 12.5 mg
- Approval
- NDA authorized generic NDA020033
- On the market since
- Apr 7, 2019
- Package NDCs
0574-0229-01- Official label
- DailyMed (National Library of Medicine), updated May 11, 2023
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