NDC 62559-414 – Benazepril Hydrochloride and Hydrochlorothiazide

Benazepril Hydrochloride 5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62559-414

Product details

Brand name
Benazepril Hydrochloride and Hydrochlorothiazide
Generic name
Benazepril Hydrochloride and Hydrochlorothiazide
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076342
Marketed since
November 7, 2022
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Benazepril hydrochloride and hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
62559-414-01100 TABLET in 1 BOTTLE (62559-414-01)Nov 7, 2022

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