NDC 68071-2823

Lisinopril and Hydrochlorothiazide 20 mg / 12.5 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-421.

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 Solco Healthcare U.S., LLC names for other drugs.

Repackaging site

Product details

Generic drug
Hydrochlorothiazide and Lisinopril: every company that makes it
Form
tablet
Strength
20 mg / 12.5 mg
Approval
ANDA ANDA076230
On the market since
Mar 12, 2015
Package NDCs
68071-2823-3 68071-2823-9
Official label
DailyMed (National Library of Medicine), updated Oct 4, 2022

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