NDC 33342-247 – Olmesartan medoxomil Amlodipine and Hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 10 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-247
Product details
- Brand name
- Olmesartan medoxomil Amlodipine and Hydrochlorothiazide
- Generic name
- Olmesartan medoxomil Amlodipine and Hydrochlorothiazide
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207088
- Marketed since
- July 18, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 40 mg/1
- Amlodipine Besylate 10 mg/1
- Hydrochlorothiazide 25 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 33342-247-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-247-07) | Jul 18, 2025 |
| 33342-247-10 | 90 TABLET, FILM COATED in 1 BOTTLE (33342-247-10) | Jul 18, 2025 |
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