NDC 62559-660 – Candesartan Cilexetil and Hydrochlorothiazide

Candesartan Cilexetil 16 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62559-660

Product details

Brand name
Candesartan Cilexetil and Hydrochlorothiazide
Generic name
Candesartan Cilexetil and Hydrochlorothiazide
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021093
Marketed since
September 26, 2018
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Candesartan Cilexetil and Hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
62559-660-9090 TABLET in 1 BOTTLE (62559-660-90)Sep 26, 2018

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