NDC 73190-078 – Olmesartan medoxomil-hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC73190-078
Product details
- Brand name
- Olmesartan medoxomil-hydrochlorothiazide
- Generic name
- Olmesartan medoxomil-hydrochlorothiazide
- Labeler
- AvKARE
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA021532
- Marketed since
- July 14, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Olmesartan medoxomil-hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 73190-078-90 | 90 TABLET, FILM COATED in 1 BOTTLE (73190-078-90) | Jul 14, 2026 |
Other Olmesartan medoxomil-hydrochlorothiazide products
- 42291-924 Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · AvKARE
- 42291-925 Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · AvKARE
- 42291-926 Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · AvKARE
- 73190-079 Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · AvKARE
- 73190-080 Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · AvKARE
- 72205-147 Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC
- 72205-148 Olmesartan Medoxomil 40 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