NDC 72205-148 – Olmesartan medoxomil-hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC72205-148
Product details
- Brand name
- Olmesartan medoxomil-hydrochlorothiazide
- Generic name
- Olmesartan medoxomil-hydrochlorothiazide
- Labeler
- Novadoz Pharmaceuticals LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA217398
- Marketed since
- September 26, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 40 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Olmesartan medoxomil-hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 72205-148-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72205-148-30) | Sep 30, 2025 |
| 72205-148-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72205-148-90) | Sep 30, 2025 |
| 72205-148-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (72205-148-99) | Sep 30, 2025 |
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- 72205-147 Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-149 Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC