NDC 49884-790-09
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 10 mg/1
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide · TABLET, FILM COATED
This is a combination blood pressure medication that contains three active ingredients: olmesartan (an angiotensin receptor blocker), amlodipine (a calcium channel blocker), and hydrochlorothiazide (a thiazide diuretic). It is taken by mouth as a tablet to help lower blood pressure in patients with hypertension.
Key Facts
- Brand Name
- olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- Generic Name
- olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- NDC Code (Package)
49884-790-09- NDC Code (Product)
49884-790- Manufacturer
- Par Health USA, LLC
- Strength
- 10 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA206137
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 10/26/2016
Recall History
No Recall HistoryNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.