NDC 31722-887 – Olmesartan medoxomil and hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-887
Product details
- Brand name
- Olmesartan medoxomil and hydrochlorothiazide
- Generic name
- Olmesartan medoxomil and hydrochlorothiazide
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209199
- Marketed since
- July 25, 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 And Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-887-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-887-30) | Jul 25, 2025 |
| 31722-887-32 | 10 BLISTER PACK in 1 CARTON (31722-887-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jul 25, 2025 |
| 31722-887-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-887-90) | Jul 25, 2025 |
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