NDC 63187-347

Losartan Potassium and Hydrochlorothiazide 25 mg / 100 mg tablet, film coated

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7368.

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 Teva Pharmaceuticals USA, Inc. names for other drugs.

Repackaging site

Product details

Generic drug
Hydrochlorothiazide and Losartan: every company that makes it
Form
tablet, film coated, oral
Strength
25 mg / 100 mg
Approval
ANDA ANDA077157
On the market since
Apr 6, 2010
Package NDCs
63187-347-30 63187-347-60 63187-347-90
Official label
DailyMed (National Library of Medicine), updated Aug 1, 2023

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