NDC 46708-132 – Olmesartan Medoxomil
Olmesartan Medoxomil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-132
Product details
- Brand name
- Olmesartan Medoxomil
- Generic name
- Olmesartan Medoxomil
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203012
- Marketed since
- April 24, 2017
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 46708-132-10 | 100 TABLET, FILM COATED in 1 CARTON (46708-132-10) | Apr 24, 2017 |
| 46708-132-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-132-30) | Apr 24, 2017 |
| 46708-132-90 | 90 TABLET, FILM COATED in 1 BOTTLE (46708-132-90) | Apr 24, 2017 |
| 46708-132-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-132-91) | Apr 24, 2017 |
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