Drugplain

NDC 43547-424-03

Losartan Potassium and Hydrochlorothiazide 25 mg/1

losartan potassium and hydrochlorothiazide · TABLET, FILM COATED

No Recall History

Losartan Potassium and Hydrochlorothiazide is a tablet, film coated containing losartan potassium and hydrochlorothiazide at a strength of 25 mg/1. Manufactured by Solco Healthcare US, LLC.

Key Facts

Brand Name
Losartan Potassium and Hydrochlorothiazide
Generic Name
losartan potassium and hydrochlorothiazide
NDC Code (Package)
43547-424-03
NDC Code (Product)
43547-424
Manufacturer
Solco Healthcare US, LLC
Strength
25 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA204901
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
02/15/2018

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.