NDC 54868-5296
Benazepril Hydrochloride and Hydrochlorothiazide 20 mg / 25 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Sandoz Inc.'s NDC 0185-0277.
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 Sandoz Inc. names for other drugs.
Product details
- Generic drug
- Benazeprilat and Hydrochlorothiazide: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg / 25 mg
- Approval
- ANDA ANDA076631
- On the market since
- May 16, 2005
- Package NDCs
54868-5296-0- Official label
- DailyMed (National Library of Medicine), updated Jun 4, 2010
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