NDC 70518-3398-1
Losartan Potassium and Hydrochlorothiazide 12.5 mg/1
losartan potassium and hydrochlorothiazide · TABLET, FILM COATED
Losartan Potassium and Hydrochlorothiazide is a tablet, film coated containing losartan potassium and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by REMEDYREPACK INC..
Key Facts
- Brand Name
- Losartan Potassium and Hydrochlorothiazide
- Generic Name
- losartan potassium and hydrochlorothiazide
- NDC Code (Package)
70518-3398-1- NDC Code (Product)
70518-3398- Manufacturer
- REMEDYREPACK INC.
- Strength
- 12.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA204901
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 03/30/2022
Recall History
No Recall HistoryView Full Drug Page
Losartan Potassium and Hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.