NDC 0172-2083

Hydrochlorothiazide 25 mg tablet

On the label: Teva Pharmaceuticals USA, Inc..

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 Teva Pharmaceuticals USA, Inc. names for other drugs.

Product details

Generic drug
Hydrochlorothiazide: every company that makes it
Form
tablet, oral
Strength
25 mg
Approval
ANDA ANDA083177
On the market since
Jan 12, 1973
Package NDCs
0172-2083-60 0172-2083-80
Official label
DailyMed (National Library of Medicine), updated Jul 1, 2024

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