NDC 0093-5005-56
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 5 mg/1
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide · TABLET, FILM COATED
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide is a tablet, film coated containing olmesartan medoxomil, amlodipine and hydrochlorothiazide at a strength of 5 mg/1. Manufactured by Teva Pharmaceuticals USA, Inc..
Key Facts
- Brand Name
- Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
- Generic Name
- Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
- NDC Code (Package)
0093-5005-56- NDC Code (Product)
0093-5005- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- Strength
- 5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA202491
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 11/14/2016
Recall History
No Recall HistoryView Full Drug Page
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.