NDC 42571-236 – Amlodipine And Olmesartan Medoxomil
Amlodipine Besylate 10 mg/1; Olmesartan Medoxomil 20 mg/1 · Tablet · Oral
Product NDC42571-236
Product details
- Brand name
- Amlodipine And Olmesartan Medoxomil
- Generic name
- Amlodipine and Olmesartan Medoxomil
- Labeler
- Micro Labs Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207435
- Marketed since
- January 1, 2018
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 42571-236-05 | 500 TABLET in 1 BOTTLE (42571-236-05) | Jan 1, 2018 |
| 42571-236-10 | 1000 TABLET in 1 BOTTLE (42571-236-10) | Jan 1, 2018 |
| 42571-236-30 | 30 TABLET in 1 BOTTLE (42571-236-30) | Jan 1, 2018 |
| 42571-236-90 | 90 TABLET in 1 BOTTLE (42571-236-90) | Jan 1, 2018 |
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