NDC 64380-198 – Amlodipine, Valsartan, Hydrochlorothiazide

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

Human Prescription Drug

Product NDC64380-198

Product details

Brand name
Amlodipine, Valsartan, Hydrochlorothiazide
Generic name
Amlodipine besylate valsartan hydrochlorothiazide
Labeler
Strides Pharma Science Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201087
Marketed since
June 27, 2022
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, Hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
64380-198-0130 TABLET, FILM COATED in 1 BOTTLE (64380-198-01)Jun 27, 2022
64380-198-0290 TABLET, FILM COATED in 1 BOTTLE (64380-198-02)Jun 27, 2022
64380-198-03500 TABLET, FILM COATED in 1 BOTTLE (64380-198-03)Jun 27, 2022

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