NDC 71335-0152-3
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 Bryant Ranch Prepack.
Key Facts
- Brand Name
- Losartan Potassium and Hydrochlorothiazide
- Generic Name
- Losartan Potassium and Hydrochlorothiazide
- NDC Code (Package)
71335-0152-3- NDC Code (Product)
71335-0152- Manufacturer
- Bryant Ranch Prepack
- Strength
- 12.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA091629
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 10/06/2010
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.