NDC 70518-4517-0
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE 12.5 mg/1
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE · TABLET, FILM COATED
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE is a tablet, film coated containing olmesartan medoxomil and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by REMEDYREPACK INC..
Key Facts
- Brand Name
- OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
- Generic Name
- OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
- NDC Code (Package)
70518-4517-0- NDC Code (Product)
70518-4517- Manufacturer
- REMEDYREPACK INC.
- Strength
- 12.5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA204801
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 11/10/2025
Recall History
No Recall HistoryView Full Drug Page
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.