NDC 0093-5006 – Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 5 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-5006
Product details
- Brand name
- Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202491
- Marketed since
- November 14, 2016
- 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 5 mg/1
- Hydrochlorothiazide 12.5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-5006-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-5006-56) | Nov 14, 2016 |
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