NDC 70436-015 – Olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 5 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC70436-015
Product details
- Brand name
- Olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
- Generic name
- Olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
- Labeler
- Slate Run Pharmaceuticals, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210718
- Marketed since
- May 15, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 40 mg/1
- Amlodipine Besylate 5 mg/1
- Hydrochlorothiazide 12.5 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70436-015-04 | 30 TABLET, FILM COATED in 1 BOTTLE (70436-015-04) | May 15, 2025 |
| 70436-015-06 | 90 TABLET, FILM COATED in 1 BOTTLE (70436-015-06) | May 15, 2025 |
Other Olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide products
- 70436-014 Olmesartan Medoxomil 20 mg/1; Amlodipine Besylate 5 mg/1;… · Tablet, Film Coated · Slate Run Pharmaceuticals, LLC
- 70436-016 Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 5 mg/1;… · Tablet, Film Coated · Slate Run Pharmaceuticals, LLC
- 70436-017 Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 10 mg/1;… · Tablet, Film Coated · Slate Run Pharmaceuticals, LLC
- 70436-018 Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 10 mg/1;… · Tablet, Film Coated · Slate Run Pharmaceuticals, LLC