NDC 50090-7478 – OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-7478
Product details
- Brand name
- OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
- Generic name
- OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204801
- Marketed since
- June 2, 2023
- Listing expires
- December 31, 2026
- 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 And Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7478-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7478-0) | Dec 19, 2024 |
| 50090-7478-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7478-1) | Dec 19, 2024 |
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