NDC 68071-4518-9
Losartan Potassium and Hydrochlorothiazide 25 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 25 mg/1. Manufactured by NuCare Pharmaceuticals,Inc..
Key Facts
- Brand Name
- Losartan Potassium and Hydrochlorothiazide
- Generic Name
- Losartan Potassium and Hydrochlorothiazide
- NDC Code (Package)
68071-4518-9- NDC Code (Product)
68071-4518- Manufacturer
- NuCare Pharmaceuticals,Inc.
- Strength
- 25 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA077157
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 04/06/2010
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.