NDC 31722-892 – Olmesartan medoxomil, amlodipine and hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Amlodipine Besylate 5 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-892
Product details
- Brand name
- Olmesartan medoxomil, amlodipine and hydrochlorothiazide
- Generic name
- Olmesartan medoxomil, amlodipine and hydrochlorothiazide
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209242
- Marketed since
- October 6, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 20 mg/1
- Amlodipine Besylate 5 mg/1
- Hydrochlorothiazide 12.5 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-892-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-892-30) | Oct 6, 2025 |
| 31722-892-32 | 10 BLISTER PACK in 1 CARTON (31722-892-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-892-31) | Oct 6, 2025 |
| 31722-892-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-892-90) | Oct 6, 2025 |
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