NDC 63629-2239 – olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Amlodipine Besylate 5 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC63629-2239
Product details
- Brand name
- olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- Generic name
- olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206137
- Marketed since
- October 26, 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 20 mg/1
- Amlodipine Besylate 5 mg/1
- Hydrochlorothiazide 12.5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 63629-2239-1 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-2239-1) | Oct 26, 2016 |
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