NDC 31722-853 – Olmesartan Medoxomil
Olmesartan Medoxomil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-853
Product details
- Brand name
- Olmesartan Medoxomil
- Generic name
- Olmesartan Medoxomil
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205499
- Marketed since
- May 23, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Olmesartan Medoxomil 20 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 31722-853-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-853-30) | May 23, 2025 |
| 31722-853-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-853-90) | May 23, 2025 |
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