NDC 42571-247 – OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE
Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 5 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC42571-247
Product details
- Brand name
- OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE
- Generic name
- Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide
- Labeler
- Micro Labs Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207437
- Marketed since
- March 1, 2026
- 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 25 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 42571-247-05 | 500 TABLET, FILM COATED in 1 BOTTLE (42571-247-05) | Mar 1, 2026 |
| 42571-247-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (42571-247-10) | Mar 1, 2026 |
| 42571-247-30 | 30 TABLET, FILM COATED in 1 BOTTLE (42571-247-30) | Mar 1, 2026 |
| 42571-247-90 | 90 TABLET, FILM COATED in 1 BOTTLE (42571-247-90) | Mar 1, 2026 |
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