Olmesartan Medoxomil And Amlodipine Besylate And Hydrochlorothiazide 70436-0018
Product NDC
70436-0018- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 15, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA210718
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Amlodipine Besylate | 10 mg/1 |
| Hydrochlorothiazide | 25 mg/1 |
| Olmesartan Medoxomil | 40 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (70436-018-04)
90 TABLET, FILM COATED in 1 BOTTLE (70436-018-06)
Related Products
All Olmesartan Medoxomil And Amlodipine Besylate And Hydrochlorothiazide NDC codes →External Resources