NDC 72303-0848 – Olmesartan Medoxomil
Olmesartan Medoxomil 5 mg/1 · Tablet, Film Coated · Oral
Product NDC72303-0848
Product details
- Brand name
- Olmesartan Medoxomil
- Generic name
- Olmesartan medoxomil
- Labeler
- HEC Pharm USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211049
- Marketed since
- April 10, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Olmesartan Medoxomil 5 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72303-0848-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72303-0848-1) | Apr 10, 2026 |
| 72303-0848-2 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72303-0848-2) | Apr 10, 2026 |
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