NDC 71610-671-30
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 Aphena Pharma Solutions - Tennessee, LLC.
Key Facts
- Brand Name
- losartan potassium and hydrochlorothiazide
- Generic Name
- losartan potassium and hydrochlorothiazide
- NDC Code (Package)
71610-671-30- NDC Code (Product)
71610-671- Manufacturer
- Aphena Pharma Solutions - Tennessee, LLC
- Strength
- 25 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA204832
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 07/21/2017
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.