NDC 33342-285 – Amlodipine,valsartan and hydrochlorothiazide

Amlodipine Besylate 5 mg/1; Valsartan 160 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC33342-285

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

Uses, dosage, side effects and warnings for Amlodipine,valsartan and hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
33342-285-0730 TABLET, FILM COATED in 1 BOTTLE (33342-285-07)Jan 6, 2025
33342-285-1090 TABLET, FILM COATED in 1 BOTTLE (33342-285-10)Jan 6, 2025
33342-285-1210 BLISTER PACK in 1 CARTON (33342-285-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 6, 2025

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