NDC 33342-051-07
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 Macleods Pharmaceuticals Limited.
Key Facts
- Brand Name
- Losartan potassium and Hydrochlorothiazide
- Generic Name
- Losartan potassium and Hydrochlorothiazide
- NDC Code (Package)
33342-051-07- NDC Code (Product)
33342-051- Manufacturer
- Macleods Pharmaceuticals Limited
- Strength
- 12.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202289
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 05/03/2012
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.