NDC 31722-445 – Amlodipine and Olmesartan Medoxomil
Amlodipine Besylate 5 mg/1; Olmesartan Medoxomil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-445
Product details
- Brand name
- Amlodipine and Olmesartan Medoxomil
- Generic name
- Amlodipine and Olmesartan Medoxomil
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209591
- Marketed since
- February 14, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 5 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 |
|---|---|---|
| 31722-445-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-445-30) | Feb 14, 2025 |
| 31722-445-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-445-90) | Feb 14, 2025 |
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