NDC 52959-595
Benazepril Hydrochloride and Hydrochlorothiazide 10 mg / 12.5 mg tablet, film coated
On the label: H.J. Harkins Co., Inc.. It's repackaged from NDC 0185-0204, made by Eon Labs, Inc. (Benazepril Hydrochloride and Hydrochlorothiazide). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were 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 H.J. Harkins Co., Inc. names for other drugs.
Product details
- Generic drug
- Benazeprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg / 12.5 mg
- Approval
- ANDA ANDA076631
- On the market since
- Feb 11, 2004
- Package NDCs
52959-595-60- Official label
- DailyMed (National Library of Medicine), updated Dec 20, 2011
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