NDC 33342-287 – Amlodipine,valsartan and hydrochlorothiazide
Amlodipine Besylate 10 mg/1; Valsartan 320 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-287
Product details
- Brand name
- Amlodipine,valsartan and hydrochlorothiazide
- Generic name
- Amlodipine,valsartan and hydrochlorothiazide
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207299
- Marketed since
- January 6, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic
Active ingredients
- Amlodipine Besylate 10 mg/1
- Valsartan 320 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Amlodipine,valsartan and hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 33342-287-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-287-07) | Jan 6, 2025 |
| 33342-287-10 | 90 TABLET, FILM COATED in 1 BOTTLE (33342-287-10) | Jan 6, 2025 |
| 33342-287-12 | 10 BLISTER PACK in 1 CARTON (33342-287-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jan 6, 2025 |
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