NDC 70436-014-04
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide 5 mg/1
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide · TABLET, FILM COATED
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide is a tablet, film coated containing olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide at a strength of 5 mg/1. Manufactured by Slate Run Pharmaceuticals, LLC.
Key Facts
- Brand Name
- olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
- Generic Name
- olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
- NDC Code (Package)
70436-014-04- NDC Code (Product)
70436-014- Manufacturer
- Slate Run Pharmaceuticals, LLC
- Strength
- 5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA210718
- Drug Class
- Thiazide Diuretic [EPC]
- Marketing Start
- 05/15/2025
Recall History
No Recall HistoryView Full Drug Page
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.