NDC 67877-500 – Amlodipine and olmesartan Medoxomil
Amlodipine Besylate 10 mg/1; Olmesartan Medoxomil 20 mg/1 · Tablet · Oral
Product NDC67877-500
Product details
- Brand name
- Amlodipine and olmesartan Medoxomil
- Generic name
- Amlodipine and olmesartan Medoxomil
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209042
- Marketed since
- August 14, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 10 mg/1
- Olmesartan Medoxomil 20 mg/1
Uses, dosage, side effects and warnings for Amlodipine and Olmesartan Medoxomil →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 67877-500-30 | 30 TABLET in 1 BOTTLE (67877-500-30) | Aug 14, 2017 |
| 67877-500-90 | 90 TABLET in 1 BOTTLE (67877-500-90) | Aug 14, 2017 |
Recalls mentioning this NDC
- D-0712-2026 Jul 29, 2026 · Class II
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications - D-0556-2026 Jun 10, 2026 · Class II
Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications - D-0576-2025 Aug 20, 2025 · Class II
Failed Dissolution Specifications: low dissolution results
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